FCC ID: O8PSMARTPILL Capsule

Appendix: Electrical Safety SmartPill GI Monitoring System User Manual MotiliGI v3.0 Doc: 111482-01 March 2013 Appendix: Electrical Safety Copyrights Text, graphics, logos and images in this manual are the property of Given Imaging and protected by United States and international copyright laws. This Manual may not be transferred or reproduced in any form without the written permission of Given Imaging. Copyright 2006-2012 Given Imaging. All Rights Reserved. Trademarks MotiliGI and The Measure of GI Health are registered trademarks, and SmartPill and the SmartPill logo are trademarks of Given Imaging. Such marks are protected by United States common law, federal and/or international trademark laws and may not be used in violation of Given Imagings rights. Patents Certain uses and features of the products referenced herein are protected by one or more United States and international patents or have pending patent applications. Limited Warranties The SmartPill GI Monitoring System Given Imaging warrants the system* for a period of one (1) year from date of purchase, and that the components of the system* have been designed, manufactured, packaged and tested and, if properly used, are free from any defect of workmanship or materials that would materially and adversely affect their intended use. If any component of the system* fails during the period of this Limited Warranty for reasons covered by this Limited Warranty, Given Imaging, at its option, shall replace the specific failed component. This Limited Warranty does not cover failure occurring in connection with or arising out of uses not intended by Given Imaging, misuse, neglect, alteration, repair, improper installation or improper testing. Without limiting the generality of the foregoing statement, this Limited Warranty shall be invalidated if any repairs, services or modifications are made to any of the components by any person not explicitly authorized by Given Imaging. Given Imaging is not liable or otherwise responsible for any loss, damage, or expense arising, directly or indirectly, from the use of the system* or SmartPill capsule. Without limiting the generality of the foregoing statement, customers are liable for all matters beyond Given Imagings control such as handling, storage, cleaning, misuse, treatment and diagnosis. Appendix: Electrical Safety This Limited Warranty is in lieu of and excludes all other warranties, whether expressed or implied, including without limitation warranties of merchantability or fitness. Extended Warranty Options are available.

* Only the data receiver, docking station and activation fixture of the SmartPill GI Monitoring System are covered by this Limited Warranty:

The SmartPill Capsule Given Imaging warrants each Capsule is free from defects in workmanship and materials until the Capsules labeled expiration date. If Given Imaging verifies capsule failure during the warranty period for reasons covered by the Limited Warranty, Given Imaging shall replace the failed capsule. Additional Limitations The Limited Warranty does not cover software or damages due to misuse, neglect, alteration, repair, improper installation, set-up, calibration or improper testing. Given Imaging is not liable for any incidental or consequential loss, damage, or expense arising, directly or indirectly, from the use of the system or capsule. Customers are liable for all matters beyond Given Imagings control such as handling, storage, cleaning, misuse, treatment, and diagnosis. This warranty is in lieu of and excludes all other warranties whether expressed or implied warranties of merchantability or fitness. The System Computer The system computer is covered under the manufacturers warranty. Rx Only Given Imaging 3950 Shackleford Road, Suite 500 Duluth GA 30096 USA supportUS@givenimaging.com Given Imaging GmbH Borsteler Chaussee 47 D-22453 Hamburg, Germany supportEU@givenimaging.com This device complies with Part 15 of the FCC. Operation is subject to the following two conditions:

1. This device may not cause harmful interference. 2. This device must accept any interference received, including interference that may cause undesired operation. Appendix: Electrical Safety Table of Contents

............................................................................................................................................. 1 Introduction and Components ............................................................................................... 9 Using this Manual ................................................................................................................. 9 System Components ........................................................................................................... 10 SmartPill Capsule Pack ................................................................................................... 10 Capsule Operational Specifications ............................................................................... 10 SmartBar ........................................................................................................................... 10 Data Receiver ................................................................................................................... 11 Docking Station ............................................................................................................... 12 Activation Fixture ........................................................................................................... 13 System Computer and MotiliGI Software ................................................................... 13 Accessories ....................................................................................................................... 14 Use and Care of the System .................................................................................................. 16 Acronyms, Use, and Symbols ............................................................................................ 16 Acronyms ......................................................................................................................... 16 Intended Use/Indications for Use ................................................................................... 16 Contraindications for Use .............................................................................................. 16 Restricted Use .................................................................................................................. 17 Storage .................................................................................................................................. 17 Power Requirements ....................................................................................................... 17 Recycling and Disposal Instructions ............................................................................. 18 Device Markings ................................................................................................................. 18 Data Receiver Display Messages ................................................................................... 19 Risks and Safety .................................................................................................................. 20 Non-Passage .................................................................................................................... 20 Patient-Contacting Materials .......................................................................................... 21 Care, Cleaning and Maintenance ....................................................................................... 21 Data Receiver ................................................................................................................... 21 Docking Station ............................................................................................................... 22 Troubleshooting and Support ........................................................................................... 22 Setting-Up the System ........................................................................................................... 23 Getting Started .................................................................................................................... 23 Appendix: Electrical Safety Setting up the Computer ................................................................................................ 23 Preparing for a Test ............................................................................................................... 25 Before the Test Day ........................................................................................................... 25 Charging the Data Receiver ........................................................................................... 25 Preparing the Patient ...................................................................................................... 26 During the Office Visit .................................................................................................. 27 Starting a Test ......................................................................................................................... 30 Preparing the System ......................................................................................................... 30 Performing the Test Test Initiation Wizard ................................................................ 30 Step 1: Connect the Data Receiver ............................................................................... 30 Step 2: Enter Patient Information ................................................................................ 31 Creating Templates: ........................................................................................................ 33 Using Templates ............................................................................................................. 33 Step 3: Assemble Materials ............................................................................................ 34 Step 4: Activate Capsule ................................................................................................. 35 Step 5: Select Capsule ..................................................................................................... 36 Step 6: Enter Pressure Calibration Code ..................................................................... 38 Step 7: Add pH Calibration Buffer ............................................................................... 38 Step 8: Capsule pH Calibration ..................................................................................... 39 Step 9: Ingestion.............................................................................................................. 40 Step 10: Complete Discharge Checklist ....................................................................... 42 Live Monitoring Mode (optional) .................................................................................... 43 Aborting a Test Deactivating the Capsule ................................................................... 44 Ending a Test ......................................................................................................................... 45 Returning the Data Receiver ............................................................................................. 45 Downloading a Test ........................................................................................................... 45 Post Test Notes ............................................................................................................... 46 Confirming Capsule Exit ............................................................................................... 47 Analyzing the Test ................................................................................................................. 48 Introduction to the Test Analysis Wizard ....................................................................... 48 Analyzing the Test .............................................................................................................. 50 Patient Diary Events ....................................................................................................... 50 Select Capsule Ingestion ................................................................................................ 51 Appendix: Electrical Safety Gastric Acidity ................................................................................................................. 52 Procedure Deviation Additional Meal Before 6 Hours .......................................... 53 Select Gastric Emptying ................................................................................................. 55 Magnitude of pH Rise at Emptying .............................................................................. 56 Gastric Pressure Characteristics .................................................................................... 57 Small Bowel pH profile .................................................................................................. 57 Small Bowel Pressure Characteristics ........................................................................... 58 Select Ileo-Cecal Junction .............................................................................................. 59 Colonic Pressure Characteristics ................................................................................... 60 Warning: Data Collected During Capsule Low Voltage ............................................ 61 Select Body Exit .............................................................................................................. 62 Review Your Physiological Markers with MotiliGIs Markers ...................................... 64 MotiliGI-Computed Capsule Ingestion ........................................................................ 65 MotiliGI-Computed Gastric Emptying ........................................................................ 66 Absence of Gastric Emptying ....................................................................................... 67 Gastric Emptying Statistics ............................................................................................ 68 Gastric Emptying Time Evaluation .............................................................................. 69 MotiliGI-Computed ICJ ................................................................................................. 70 Small Bowel Transit Time Evaluation .......................................................................... 71 MotiliGI-Computed Body Exit ..................................................................................... 72 Absence of Body Exit ..................................................................................................... 73 Colonic Transit Time Evaluation .................................................................................. 74 Test Analysis Review ...................................................................................................... 74 Reading Test Summary Reports........................................................................................ 75 Transit Data Tab ............................................................................................................. 76 Descriptive Data Tab ...................................................................................................... 77 Interpretations Tab ......................................................................................................... 78 Properties Tab ................................................................................................................. 79 Examples of Physiological Markers .................................................................................. 79 Ingestion ........................................................................................................................... 79 Gastric Emptying ............................................................................................................ 80 ICJ ..................................................................................................................................... 81 Body Exit Time ............................................................................................................... 81 Appendix: Electrical Safety MotiliGI Features................................................................................................................... 83 MotiliGI User Interface ..................................................................................................... 83 Titlebar ............................................................................................................................. 83 Main Menus ..................................................................................................................... 83 Toolbar Icons .................................................................................................................. 83 Graph Area ...................................................................................................................... 85 Data Panels ...................................................................................................................... 85 Time Slider Control ........................................................................................................ 85 Display Tabs .................................................................................................................... 85 Status Bar ......................................................................................................................... 85 MotiliGI Keyboard Shortcuts ....................................................................................... 86 Opening a Test by the Patients Name ........................................................................ 86 Opening a Test by the File Name ................................................................................. 87 Closing a Test .................................................................................................................. 87 Exiting MotiliGI.............................................................................................................. 88 Setting General User Preferences ..................................................................................... 88 General Tab ..................................................................................................................... 88 Graph Tab ....................................................................................................................... 89 Report Tab ....................................................................................................................... 90 Creating Report Letterhead ........................................................................................... 91 Files Tab ........................................................................................................................... 92 Setting Preferences Back to Default ............................................................................. 92 Editing Patient Information .............................................................................................. 92 Changing the Graph Display ............................................................................................ 93 Selecting Data Plots ........................................................................................................ 93 Changing the Test View ................................................................................................. 94 Changing Axis Scales ...................................................................................................... 96 Analyzing Data ................................................................................................................... 97 Showing and Hiding Annotations ................................................................................ 97 Editing Patient Diary Events ......................................................................................... 97 Creating New Event Annotations ................................................................................ 98 Editing Event Annotations ............................................................................................ 98 Adding or Changing the Location of Physiological Markers .................................... 99 Appendix: Electrical Safety Viewing Transit Times ..................................................................................................100 Calculating Statistics ......................................................................................................100 Creating Output ................................................................................................................101 Generating a Report ......................................................................................................101 Exporting Data to Excel ..............................................................................................102 Exporting Images to JPEG or GIF ............................................................................104 System Administrator Tools ...............................................................................................105 Password Management ....................................................................................................105 Logging into the System Computer ............................................................................105 Logging into MotiliGI ..................................................................................................106 MotiliGI Security ..............................................................................................................106 Security Tab ...................................................................................................................106 Backing Up Patient Files ..............................................................................................107 Installing Software ............................................................................................................108 MotiliGI Administrator ................................................................................................108 Installing Software from a CD ....................................................................................109 Installing Software from a File on the System Computer Hard Drive ...................109 Uninstalling MotiliGI ....................................................................................................110 Installing MotiliGI .........................................................................................................110 Appendix: Electrical Safety .................................................................................................112 Index ...................................................................................................................................116 Contacting Given Imaging ..............................................................................................119

Appendix: Electrical Safety Using this Manual Complete user training and read this manual before running the SmartPill System. This manual contains important safety information and contraindications. This manual makes use of 2 special notations: Warning and Caution, the meanings of which are:

Warning Potentially hazardous situations which could result in serious adverse reactions (death or serious injury) or serious safety hazards to users and patients. All warnings are boxed. Caution Potentially hazardous situations which could result in minor or moderate injury or damage to the equipment or other property. Appendix: Electrical Safety System Components SmartPill Capsule Pack Each capsule pack contains a single-use capsule, calibration buffer, instructions for use and a patient diary. The capsule measures pressure, pH, and temperature to determine transit times of the stomach, small bowel, and colon. Transit times derived by capsule motility procedures provide alternatives to other tests such as gastric emptying scintigraphy, whole gut scintigraphy, and radio-opaque markers. Caution Do not use a SmartPill capsule if it has been dropped as this may affect function. Capsule Operational Specifications Specification Attribute 0-99 mmHg 5 mmHg Pressure Accuracy 100-350 mmHg 10% of applied pressure Pressure Range 0-350 mmHg 0.5 pH units pH Accuracy 19 pH units pH Range Temperature Accuracy 1C (between 20 42C) 434.2 MHz (radiating between 426 445 MHz) Transmission Frequency Capsule and Data Receiver, >5 days Battery Life Weight 4.5 grams 26 x 13mm Size SmartBar The SmartBar is a standardized meal that is ingested immediately before capsule ingestion. To accurately measure gastric emptying patients must consume a standard meal immediately before ingesting the capsule. Appendix: Electrical Safety Data Receiver The data receiver records biomedical data sent by the capsule. It is worn by the patient on a belt clip or a lanyard (around the neck). The data receiver features an Event button that when pushed places a marker in the electronic data. A patient diary for recording the time and reason for the event button use is stored on the backside of the receiver. The data receiver weighs approximately 225g (0.5 lb). Caution Use only the SmartPill Docking Station (REF 50100400) to charge and download data from the receiver. Figure 1 Feature A - Data Display B Backlight Control Button C Event Button D Belt Clip and Lanyard E Patient Diary Description See Data Receiver Display Modes, Page 19 for more details. The backlight button turns on a light, enabling the display to be read in low light conditions. The backlight button is also used to turn the data receiver off. The backlight button and event button (described below) must be simultaneously depressed for 5 seconds to turn the data receiver off. The Event button turns the data receiver on. Patients press the event button when engaging in an event (light exercise, eating, going to the bathroom, sleeping, abdominal discomfort, pain, etc.) or experiencing any symptom which the clinician believes may affect GI physiology and may be of interest. Pressing the event button inserts a marker in the test data record. The data receiver is equipped with a belt clip and supplied with a lanyard. The patient has the choice of clipping the data receiver on a waist belt or wearing the data receiver suspended from a lanyard. The patient diary is to be used by the patient to record events, activities and symptoms listed in the patient instruction sheet, and the date and time the events occurred. The entries in the patient diary should correspond to the event button markers inserted into the test data record when the event button is pressed. Appendix: Electrical Safety Docking Station The docking station establishes electronic communication between the data receiver and the system computer for data download and serves as a charging stand for the data receiver. The docking station weighs approximately 200 grams (0.45 lbs). Caution Use only the Power Supply (REF 30100900) supplied with the SmartPill Docking Station. Figure 2 Feature A LED Light B DC Power Connector C USB Connector Description Indicates the state of data receiver. See table below. Provides a connection point for the power supply. Provides a connection point for the USB cable, connecting the docking station to the system computer. Appendix: Electrical Safety LED Color Red Yellow Green Off State Charging A charging circuit fault has occurred Fully charged

Docking station is not connected to an AC power source

Receiver is not fully connected to the docking station

Docking station or data receiver are in thermal shutdown Action Recommended Continue charging until the LED turns green. Undock and then re-dock the data receiver in the docking station. If the yellow light persists contact technical support. The data receiver is ready for use.

Connect the docking station to a source of AC power.

Undock and then re-dock the data receiver in the docking station.

Contact technical support for assistance. Activation Fixture The activation fixture turns the capsule on and off using strong magnets that interact with the capsules internal power switch. Warning Individuals with pacemakers should not come within one (1) foot of the SmartPill activation fixture. The fixture contains strong magnets that could interfere with pacemaker operation. Warning Do not store the SmartPill Activation Fixture in the same room with or a room adjacent to MRI equipment. The fixture contains strong magnets and could become a dangerous projectile. Caution Keep the SmartPill Activation Fixture more than two (2) feet from magnetic media and computer monitors. Caution Do not store unused capsules within one (1) foot of the SmartPill Activation Fixture. Stray magnetic fields from the activation fixture may activate the capsule. System Computer and MotiliGI Software MotiliGI software comes installed on the system computer. MotiliGI receives and processes downloaded data from the data receiver, stores test data, provides data analysis tools, and graphically displays test results. MotiliGI features algorithms that calculate GET, SBTT, CTT, WGTT, and motility indices of the antrum and Appendix: Electrical Safety duodenum. An optical mouse is supplied with the system computer. An electronic copy of this user manual is included in the software. Caution Use MotiliGI only on the system computer supplied with the SmartPill GI Monitoring System. Installing and operating MotiliGI on another computer is not recommended or supported by SmartPill Corporation. Caution Do not use the vertical pipe (|) character in text fields or the software will remove it. Minimum System Computer Requirements Manufacturer Operating System Dell (preferred), IBM, HP, Toshiba Any of the following 32-bit Microsoft Windows versions:

XP Professional Service Pack 3 (recommended)

Windows Vista Business

Windows Vista Ultimate

Windows 7 Professional (recommended)

Windows 7 Ultimate System does not work with 64-bit operating systems 100 megabytes of available space for the MotiliGI application and 10 gigabytes of available space for test files (recommended) 1 open USB port CD/RW Drive; printer is optional Pentium IV 1 Gigahertz (GHz) or higher 1 gigabyte (GB) of RAM or 1280 x 800 resolution widescreen aspect ratio (recommended) 96 dpi 32-bit color Microsoft .NET Framework 1.1 SP 1 Adobe Acrobat 7.0.8 or later Hard Drive Communication Port Peripherals Processor Memory Display Other Accessories Your starter kit includes the acceosories below:

Accessory Starter Kit Backpack Belt Clips and Lanyards User Manual USB Cable Power Cord Patient Instruction Sheets Power Adaptor (non US systems) Description A protective backpack that holds the system components. Attach to the back of the data receiver. Complete the user training and read this manual before running the SmartPill System. The user manual contains important safety information. Connects the docking station to the system computer. Powers the docking station Instruction sheets to send home with the patient Modifies the power supply. Warning Do not connect items to the SmartPill GI Monitoring System that are not part of the system. Appendix: Electrical Safety Appendix: Electrical Safety

Acronyms, Use, and Symbols Acronyms GET SBTT CTT SLBTT Gastric emptying time Small bowel transit time Colonic transit time Combined small and large bowel transit time Whole gut transit time WGTT Intended Use/Indications for Use The SmartPill GI Monitoring System measures whole gut and regional gut (stomach, small bowel, and colon) transit times. Measurements of gastrointestinal (GI) tract transit times are used for evaluating motility disorders. The system measures pH, pressure, and temperature throughout the GI tract. Pressure contraction data from the antrum and duodenum can be used to calculate motility indices. Suspected disease or condition to evaluate Gastroparesis Indicated Measurement GET Use Delayed gastric emptying is implicated in such disorders as idiopathic and diabetic gastroparesis and functional non-ulcer dyspepsia. Aids in differentiating slow and normal transit constipation. A surrogate measure of colonic transit in patients with chronic constipation when CTT alone cannot be determined. Chronic constipation CTT SLBTT Caution Do not use in patients younger than 18 years old. Contraindications for Use Do not use in patients with these diseases or conditions:

Appendix: Electrical Safety

history of gastric bezoar

swallowing disorders

suspected or known strictures, fistulas, or physiological/mechanical GI obstruction

GI surgery within the past 3 months

severe dysphagia to food or pills

Crohns disease or diverticulitis

implanted or portable electro-mechanical medical device such as a cardiac pacemaker, defibrillator or infusion pump

younger than 18 years old. Data transmission from the capsule to the data receiver is influenced by patient BMI. Significant data dropout can occur in severely obese patients (>40 BMI). Restricted Use Caution The SmartPill GI Monitoring System equipment is not suitable for use in the presence of flammable anesthetic mixture with air or with oxygen or nitrous oxide. Not for use with oxygen or oxygen-enriched atmospheres. Storage Store SmartPill GI Monitoring System components and capsules at ambient room temperature (-1540C) and humidity (rH 3090%). Caution Do not expose the capsules to UV light. UV light can permanently damage the pH sensor. Caution Do not store capsules within 30cm (1 foot) of the activation fixture. The fixtures magnetic field could inadvertently activate the capsules. Power Requirements System Computer Docking Station Capsule Data Receiver 110/220 VAC, 5060 Hz May require the use of a power plug adapter 110/220 VAC, 5060 Hz May require the use of a power plug adapter none 3.1 VDC self-contained batteries 8.4 VDC, self-contained, none Appendix: Electrical Safety rechargeable batteries Recycling and Disposal Instructions

Recycle the data receiver and docking station following the local, regional, and national regulations for electronic devices.

The capsule contains silver oxide batteries. Recycle unused capsules following the local, regional and national regulations for electronic devices.

Dispose of used capsules following local, regional and national regulations for disposing of human excrement.

The calibration buffer contains sodium citrate, a common food preservative. Dispose of used buffer following local, regional, and national disposal regulations. Device Markings Caution, consult accompanying documents Consult directions for use US FCC compliance Prescription use only Recycle. Dispose of properly Single use only. Do not reuse Part or catalog number Manufacturer Date of manufacture Use by YYYY-MM Lot number Minimum and maximum storage temperature Caution: Strong magnet Warning: Keep away from pacemakers BF 0123 IP57 Appendix: Electrical Safety Type BF equipment CE marking and notified body number Authorized representative Sufficient for one test Ingress protection rating Serial number Fragile Keep dry Data Receiver Display Messages Looking for capsuleappears during test initiation before the receiver receives the first data packet from the capsule. Locked onto capsuleappears after the data receiver receives first data packet from the capsule. Test in progressappears when a test is in progress and the data receiver is turned off and back on. Data to downloadappears when the data receiver stops collecting data and has data to be downloaded. Time Capsule and data receiver status icons /

[X] indicates a failure Signal Strength Pressure pH Indicates the data receiver is writing data from the capsule. Indicates the event button is pushed. The capsules data was received. / [X] indicates the data was not received. Appendix: Electrical Safety The receivers battery life. 1 bar = 1 day of battery life. 3 bars = 3+ days. Risks and Safety Warning This device does not differentiate between slow motility and functional outlet obstruction. Non-Passage Risks associated with capsule ingestion and transit are minimal. The primary hazard is capsule retention. Retention incidence, as determined by a review of published studies of capsule endoscopy in adults, is estimated as 0.75% in patients without known stenosis and 21% in patients with known stenosis. Stenosis and strictures can be complications in inflammatory bowel disease. If you suspect a delay in passage and the Capsule is located in the stomach, a pro-

motility drug could be administered to assist in emptying the capsule from the stomach. Alternatively, endoscopy could be performed in order to retrieve the capsule. If located in the colon, laxative therapy could be administered to facilitate capsule movement, or a colonoscopy could be performed in order to retrieve the capsule. Adverse events reported in clinical studies involving the SmartPill are listed below. Reported Adverse Events in Clinical Study Subjects (n=484) Number of Events Reported Number not related to the device Number probably not related to the device Number possibly related to the device Number definitely related to the device 59 33 17 5 4 Reported Adverse Events in Clinical Practice In clinical practice since 2007, the company identified 25 events whose circumstances suggested a potentially reportable event to regulatory authorities. After investigation and follow up, seven of these events were deemed reportable including three instances of esophageal retention, one gastric retention and three small bowel retentions. Surgery was required for resolution in one instance of capsule small bowel retention that led to identification of a stricture. A bowel prep resolved the second instance of small bowel retention, and the third resolved with fluids and bed rest. Capsule retention in the stomach was resolved endoscopically. Two of the retentions in the esophagus were resolved endoscopically and in the third instance the patient vomited and then performed a self-applied Heimlick maneuver to expel the capsule. There Appendix: Electrical Safety was one additional esophageal retention, eight gastric retentions, four small bowel retentions and five colonic retentions. These resolved either without intervention or with endoscopy/colonoscopy. Patient-Contacting Materials Patient-contacting materials include polyurethane, a polyurethane-polycarbonate blend, Teflon coated with polyhema, an ISFET pH sensor, epoxy and UV-cured adhesive. All patient contacting materials have been tested for biocompatibility and have been found non-toxic, non-sensitizing, and non-irritating. The device does not contain natural rubber latex. Care, Cleaning and Maintenance Caution Do not reuse capsules. The capsule is a single-use, disposable item. Caution Do not immerse the data receiver in water or other liquids. Immersion damages internal electrical components resulting in data receiver inoperability. Caution Do not immerse the docking station in water or other liquids. Immersion damages internal electrical components and could result in electrical shock. Caution The data receiver, docking station, power supply, and capsule are not user serviceable. Data Receiver Clean and disinfect the outside surfaces of the data receiver after each patient use. 1. Turn off data receiver by simultaneously depressing the backlight button and event button for 5 seconds. 2. Wipe outside surfaces with a cloth dampened (not saturated) with a mild detergent and water. Suitable detergents include dishwashing detergent (e.g., Joy, Dawn, Palmolive) solutions, or laboratory glassware cleaners such as Alconox. 3. Wipe dry. 4. Disinfect by wiping outside surfaces with a cloth dampened (not saturated) with disinfectant. A solution of 10% household bleach can be used as a disinfectant. 5. Wipe dry. 6. Wait at least 5 minutes after cleaning and disinfection before turning the data receiver on or placing it in the docking station. 7. Conduct a preventive maintenance inspection. Check for cracks or damage. Shake the data receiver and listen for detached batteries. Do not use the data receiver if the case is cracked or damaged, or a rattling can be heard. Appendix: Electrical Safety Caution Do not attempt to replace batteries in the data receiver. Docking Station 1. Unplug docking station from the power supply. 2. Dust the surfaces of the docking station with a soft, dry cloth. Do not use water or liquids. 3. Clean the gold connector pins with a swab and Isopropyl alcohol. 4. Conduct a preventive maintenance inspection. Check for cracks or damage. Do not use the docking station if the case is cracked or damaged. Caution Do not use the components of the system with any other equipment. Troubleshooting and Support Contact technical support if you have a problem setting up or operating the system:

For swift and direct support, please be prepared to answer the following questions:

What version of MotiliGI are you using? To determine what version you are using:

Select Help > About.

Refer to the version printed on the MotiliGI CD.

What operation or steps did you take before the problem occurred?

What operations or steps did you take after the problem occurred?

What is the exact error message that appeared?

If you have trouble with a capsule or other hardware component, have the components lot and serial numbers ready. These numbers are on labels affixed to the hardware component or packaging. Appendix: Electrical Safety

- Getting Started 1. Remove the data receiver, docking station, activation fixture, USB cable, power adapter, and power cord from the starter kit case. 2. Unpack the system computer and power supply from its shipping container. Connect the computer to a source of AC power. Setting up the Computer 1. To login to the System Computer, enter the information below. User Name Password 12345 sgims1 2. Ensure the system computer has the correct date, time, language and regional settings. Changing the System Computer Date, Time, Language and Regional Options 1. Select Start > Control Panel > Clock, Region and Language 2. Change the desired settings. Changing certain settings may require you to reboot the system computer. Launching MotiliGI (for the first time) 1. Open the MotiliGI software:

on the desktop.

Click

Select Start > All Programs > SmartPill folder > MotiliGI. 2. When launching MotiliGI for the first time, the MotiliGI License Agreement will appear. Review and click I Agree. You must accept the terms and conditions in order to run MotiliGI. 3. The MotiliGI Configuration appears. Enter an identification number or word (e.g. 001 or Main Office) to identify SmartPill tests run at your particular office.

If your institution or practice has more than one office, you may wish to use this feature to identify at which office a specific test was conducted. Appendix: Electrical Safety 4. Click OK. You will be asked to confirm the clinic identification number you entered; click Yes to proceed to the First Login Sequence screen. 5. Click OK. The administrator user login screen appears. 6. Create a username and password for the administrator account for MotiliGI. The username and password must contain a minimum of 5 alphanumeric characters. 7. Verify the password by re-entering it, and click Login. You will be required to enter this username and password each time you start the program. The MotiliGI Start-Up screen appears. Connecting the Docking Station to the System Computer 1. Connect the docking station to an AC power source using the power cord. 2. Connect the docking station to the system computer using the USB cable. 3. Turn the data receiver on by depressing the event button. 4. Dock the data receiver by placing it in the docking station cradle. Push down on the top of the data receiver to ensure the data receiver is fully docked. 5. Confirm the system computer and docking station are communicating by noting the presence of the data receiver connected icon horizontal bar at the bottom of the MotiliGI user interface).

If you observe the receiver communication disabled in the MotiliGI status bar (the and test state unknown icons, either the docking station is not properly connected to the system computer, or the data receiver is not fully docked. Reseat the data receiver in the docking station and ensure the docking station is connected to both the computer and a power supply. The test state unknown icon will disappear once the connection is established. If it does not disappear, contact Technical Support for assistance. 6. Before starting a test, fully charge the Data Receiver. See Chapter 4: Charging the Data Receiver for instructions. Appendix: Electrical Safety

Before the Test Day Fully charge the data receiver the day or night before starting a test. Charging can take up to 5 hours. Charging the Data Receiver 1. Ensure that the data receiver is off. If any characters appear on the display, turn off the data receiver by simultaneously pressing the 2 buttons on the front of the unit for approximately 5 seconds. Caution The data receiver must be turned off during charging. Charging the data receiver while turned on results in a partial charge. You may lose test data. 2. When the back light dims, release both buttons. 3. Plug the docking station into an electrical outlet. If necessary, use a power adapter. 4. Firmly push the data receiver into the docking station to initiate charging. The docking stations LED turns red. Figure 3

Allow up to 5 hours for the data receiver to fully charge.

The docking stations LED turns green when the data receiver is fully charged. Caution Charging or recharging the data receiver with a power source other than the SmartPill power supply may permanently damage the data receiver, docking station, or system computer and will void the product warranty. Appendix: Electrical Safety Preparing the Patient Before the Office Visit 1. Review these requirements and restrictions with the patient. The test requires fasting for accurate results. Schedule 24 hours before the test 8 hours before the start of the test 6 hours after the start of the test Restriction Do not consume alcohol. Do not eat or drink. Do not use tobacco. Do not use tobacco. Do not eat. Do not sleep. Do not consume alcohol. 2. Review the use of medications with the patient. Stop medications that alter motility or gastric pH. Examples of medications are provided below.

Unless the patient is well stabilized (condition and dose has been stable for 3 months or more), discontinue these medications prior to the start of the test. Schedule 7 days before the tests Type Proton pump inhibitors 48 Hours 48 Hours 48 Hours 48 Hours 48 Hours 48 Hours 24 Hours Histamine2 blockers Motility-altering medications Antiemetics & 5HT3 anatagonists Macrolides Anticholinergics 5HT4 partial agonists Antacids Examples Omeprazole, Lansoprazole, Nexium Zantac Cisapride, Domperidone, Metoclopramide

(Reglan) Zofran, Kytril Erythromycin, Zithromycin Phenergan, Compazine Zelnorm Maalox, Mylanta, Appendix: Electrical Safety Rolaids

Insulin-dependent diabetic patients must take half of their normal morning dose of insulin and monitor glucose levels according to normal routines. 3. Review SmartBar ingredients and rule out any food allergies.

The SmartBar contains a small amount of gluten.

The SmartBar does not contain lactose.

The SmartBar does not contain nuts but is manufactured in a plant that processes nuts. SmartBar Ingredients Nutritional Composition

(in % of weight) Granola (Rolled Oats, Evaporated Cane Juice, Expeller Pressed Canola Oil, Defatted Wheat Germ, Oat Flour, Brown Rice Syrup, Molasses, Salt, Natural Flavor, Soy Lecithin), Whey Crisp, Rice Syrup, Corn Syrup, Whey Protein Isolate, Invert Sugar, Puffed Wheat, Apples, Maltodextrin, Sorbitol, Apple Juice Concentrate, Partially Hydrogenated Vegetable Oil (Cottonseed, Soybean), Honey, Natural and Artificial Flavor, Salt, Vanilla. 66% carbohydrate 3% fiber 17% protein 2% fat 243 kcal If necessary, an egg based meal can be substituted for SmartBar. You must have a microwave to prepare this meal. Ingredients cup (120 g) Egg Beaters, equivalent to the volume of 2 large egg whites; 60 kcal 2 slices of bread; 120 kcal 1.5 Tbsp. (30 g) strawberry jam; 75 kcal cup (120 ml) water Caution To accurately measure regional gut transit times the patient must consume either SmartBar or the egg based meal immediately before ingesting the capsule. During the Office Visit 1. Ensure the patient has adhered to restrictions required before the test. 2. Provide printed instructions (included in starter kit) to the patient. Additional copies can be purchased. 3. Review the schedule, restrictions, and use of medications with the patient. Inform the patient that failure to follow these instructions may invalidate the test. Schedule Restriction 6 hours after ingesting the capsule

Do not eat.

Do not take medication. During the entire test Appendix: Electrical Safety

Do not use tobacco.

Do not consume alcohol.

If you are diabetic, monitor glucose levels and follow your personal treatment plan. If you are unsure, contact the doctor who manages your diabetes.

Avoid vigorous exercise such as sit-ups, abdominal crunches, and prolonged aerobic activity (greater than 15 minutes).

Do not wear the data receiver while bathing or showering.

Do not use laxatives, bowel cathartics, anti-diarrhea medications, alcohol and other drugs or medications that affect motility until after the capsule passes. 4. Instruct the patient to keep the receiver as close to the abdomen as possible except while bathing or showering:

Positioned on a belt

Suspended by a lanyard Caution Instruct patients not to use the lanyard when sleeping Caution Eating anything (except limited quantities of water) before the capsule has emptied will delay gastric emptying of the test meal and invalidate results. 5. Instruct the patient on the use of the patient diary and the data receivers event button. Every time the patient presses event, the patient must record the time displayed on the data receiver and a brief description of the event or activity in the diary. Patients must press event for all bowel movements. Pressing event:

Marks bowel movements which are useful for verifying capsule exit.

Marks other events and symptoms which may be useful when reviewing test data.

Adds an event marker to the electronic data record. Other events and symptoms you may ask the patient to mark and enter in the patient diary include:

eating a meal getting up in the morning; going to bed at night cramping or pain nausea passing gas vigorous exercise or activity Resumption of Normal Routine 6. Review these instructions and warnings with the patient. Appendix: Electrical Safety

Patients may resume a normal diet 6 hours after swallowing the capsule.

Except for restrictions noted on the Patient Instructions Sheets, patients may resume normal activities when released from your office. Warning Magnetic Resonance Imaging (MRI) must not be performed on a patient who has ingested the capsule until capsule passage is confirmed by the physicians review of the MotiliGI graph or abdominal x-ray. An MRI test performed with an ingested capsule may result in damage to the GI tract. Warning Instruct the patient to contact your office if he or she experiences acute pain, sudden nausea, or vomiting beyond his or her typical pattern within 5 days of ingesting the capsule as these symptoms could indicate bowel obstruction. Scheduling a Follow-up Office Visit 7. Schedule a visit to return the data receiver 4-5 days (96-120 hours) from the start of the test. Appendix: Electrical Safety

Preparing the System Perform these steps immediately before or after a patients arrival at the office. 1. Turn on the system computer. 2. Open MotiliGI:

on the desktop.

Click

Select Start > All Programs > SmartPill > MotiliGI. 3. If prompted, enter a username and password. Click OK. The main startup screen appears. Performing the Test Test Initiation Wizard Step 1: Connect the Data Receiver Caution Do not close MotiliGI while operating the Test Initiation Wizard because data can be lost. Complete or cancel the Wizard first. Caution You may cancel the wizard any time. However, a capsule exposed to the pH calibration buffer must be ingested within 2 hours or discarded. 1. Follow the prompts. Check the results:

Component Docking stations LED Success Green Data receiver display System Computer 2 beeps The Looking For Capsule message appears.

These icons appear in the lower-right corner of the screen:

Troubleshooting

Red The data receiver may not be fully charged. See Chapter 4:

Charging the Data Receiver.

Yellow Undock and re-dock the data receiver in the docking station. If the yellow light persists, contact SmartPill Technical Support. LCD is blank Turn on the data receiver by pressing the event button.

No beeps

Check the computers sound level.

Undock and re-dock the data receiver in the docking station. If there are still no beeps, contact Technical Support.

The Receiver is Not Fully Charged message appears. The charge is insufficient for a 5-day test.

Appendix: Electrical Safety

Replace the data receiver with a fully charged receiver.

Allow additional charging time for the current receiver. The data receiver must be turned off during charging. Charging the data receiver while turned on results in a partial charge. You may lose test data. 2. Click Next >. Step 2: Enter Patient Information Patient information becomes a permanent part of the patients MotiliGI record. General Tab

*indicates a required field 1. Enter the required information. Contraindications Tab You must view this screen. 2. Complete the applicable fields. Appendix: Electrical Safety Depending on your selections, other screens may appear. For example, an override screen for a contraindication or caution may appear.

(Optional) Enter notes and click Physician Ok.

(Optional) Click End Test. 3. Proceed to the optional tabs below or click Next >. Optional Tabs: Prior GI Procedures, Allergies and Medications, Symptoms Entering information in these tabs is optional. The symptoms tab includes a selection of ICD9 and ICD10 codes. Appendix: Electrical Safety Creating Templates:

To save time you can create text descriptions that are saved in MotiliGI. These text templates can be reused from patient to patient. Text descriptions saved this way are called templates. We recommend creating general templates with blank lines to indicate where patient specific information can be inserted. 1. Click Create Template. a. Enter a title for the prior abdominal surgery or implanted device. Examples:

b.

Appendectomy

Gastric stimulator

(Optional) Click in the text field under the title. Enter descriptive details. Examples:

Date:______________

Name of the surgeon:___________________ 2. Click Save Template. Using Templates for saved templates. 1. Click 2. Select a template. Insert any patient specific information. 3. Click to move information to the patient record.

(Optional) To remove information from the patients record, select it and click Remove Entry. The templates remains in the Template list. To delete the selection, click Delete Template. Appendix: Electrical Safety Step 3: Assemble Materials 1. Follow the prompts.

The capsules instructions for use are in the inside pocket of the capsule pack. 2. Click Next >. Step 4: Activate Capsule Appendix: Electrical Safety 1. Follow the prompts. 2. Figure 4 - Capsule Activation Window Caution Once the capsule is activated, keep the capsule at least one (1) foot away from the activation fixture. If the capsule is kept near the activation fixture, stray magnetic fields from the activation fixture may deactivate the capsule. 3. Confirm the capsule has activated:

Observe the data receivers display for at least 1 minute. The message Locked onto Capsule and the capsules serial number will appear on the data receiver for approximately 4 seconds. Appendix: Electrical Safety

The data receivers display then indicates the capsules data:

Capsule Serial number SS = signal strength P = pressure The capsules data was received. / [X] = The data was not received. icon appears in the lower-right corner of MotiliGI: .

The If the capsule did not activate, repeat the procedure. 4. Click Next >. 5. If you wish to deactivate the test, see Aborting a Test Deactivating the Capsule, Page 44. Step 5: Select Capsule All activated capsules (ingested or not yet ingested) within range of the data receiver appear1. This process may take up to 1 minute. 1 The data receiver can detect the capsule in open air (not ingested) at distances of up to 40 feet. Appendix: Electrical Safety 1. To select the capsule you activated, click the row that matches the capsule containers serial number. An arrow indicates your selection.

If the software does not detect the capsule within a minute, observe the data receivers display to confirm the capsule is active.

If the capsule is activated the data receiver displays this data during a test. Time Capsule and data receiver status icons /

[X] indicates a failure Signal Strength Pressure pH 2. Click Next >. Indicates the data receiver is writing data from the capsule. Indicates the event button is pushed. The capsules data was received. / [X] = The data was not received. The receivers battery life. 1 bar = 1 day of battery life. 3 bars = 3+ days. Step 6: Enter Pressure Calibration Code 1. Locate the calibration code found on the lid of the capsule container. Enter the code. Appendix: Electrical Safety 2. Click Next >. Step 7: Add pH Calibration Buffer Caution Once exposed to buffer, the capsule must be ingested within 2 hours or discarded. Confirm that the patient is available and prepared to proceed with the test before you begin Step 7. 1. Put gloves on and follow the prompts. Caution Wear gloves when handling the capsule. Do not touch the calibration buffer or capsule with your finger as this could cause an electrostatic charge. Appendix: Electrical Safety Caution The orientation of the capsule in the capsule container is important. When reinserting the capsule, ensure the pH sensor is in the same orientation relative to the diamond-shaped window of the capsule container. C B A Figure 5 - Capsule Orientation A Capsule pH sensor B Buffer filling channel C Diamond shaped window Do not discard the capsule containers cover. The cover contains information that is needed if the test cannot take place as planned or assistance from Technical Support is required. 2. Click Next >. Step 8: Capsule pH Calibration No action is necessary. The software checks the status of the capsule and data receiver during this step. Appendix: Electrical Safety

Calibration normally takes less than 3 minutes, but may take up to 15 minutes.

During calibration, it is normal for fluctuations in the pH value to occur. Calibration is complete when all these signals appear:

The pH value stabilizes at 6.0.

The pH Calibration Complete message appears.

The MotiliGI status bar icon data receiver is recording information from the capsule. indicates the capsule is ready for use and the If the capsule does not calibrate within 15 minutes, this message appears: pH Calibration Timeout. 1. Ensure the capsule is immersed in buffer. 2. Click Back. 3. Click Next. The calibration process reinitiates.

If the calibration fails after 2 attempts contact Technical Support. Step 9: Ingestion 1. Follow the prompts. Record the time of completion in the patient diary. Caution The meal must be eaten immediately before capsule ingestion. Appendix: Electrical Safety Caution To avoid loss of data during Step 9.2, avoid separating the capsule and data receiver by more than 5 feet. The data receiver records biomedical data from within the patients GI tract. Every few seconds, the pH and pressure readings update on the data receivers display. Dispose of the pH calibration buffer following all applicable regulations. The buffer is a solution of sodium citrate pH 6.0. 2. Click Next >. Step 10: Complete Discharge Checklist Appendix: Electrical Safety 1. Review the discharge checklist with the patient. Instruct the patient to wait 3 minutes in the bathroom before flushing the toilet after each bowel movement. Explain that to confirm body exit, the patient must let the capsule communicate with the data receiver after bowel movements. 2. Review these warnings:

Warning Magnetic resonance imaging (MRI) must not be performed on a patient who has ingested the capsule until capsule passage is confirmed by physician review of the MotiliGI graph or abdominal x-ray. An MRI test performed with an ingested capsule may result in damage to the GI tract. Warning Instruct the patient to contact your office if he or she experiences acute pain, sudden nausea, or vomiting beyond his or her typical pattern within 5 days of ingesting the capsule as these symptoms could indicate bowel obstruction. Warning If you suspect bowel obstruction, treat consistent with your management of a foreign object causing obstruction. Consider an abdominal x-ray to determine if the capsule is retained and its location within the GI tract. 3. Schedule an appointment for the patient to return the data receiver. The capsule typically passes naturally within 25 days after ingestion depending upon the patients condition. Appendix: Electrical Safety Guidelines:

Indication for Use Measuring GET Measuring WGTT Return Data Receiver After 24-48 hours 25 days 4. Check the box I have completed the patients discharge. 5. Click Finish. The Patient Information screen appears. 6. Do any of the following:

Enter notes regarding the patients capsule ingestion.

Close MotiliGI.

Use Live Monitoring mode to view live data while the patient is still in the office. Live Monitoring Mode (optional) You may view live data from the capsule while the patient is still in the office. Prerequisites:

The test has begun.

The docking station is connected to the system computer.

The data receiver is in the docking station. 1. Click or select Action > Live Monitoring. The Live Monitoring control panels appears on the right. It may take several minutes for sufficient data to be captured before the MotiliGI graph begins to show a noticeable progression of pressure, pH, and temperature data values. Caution The patient must remain in close proximity of the docked data receiver during live monitoring. If the patient moves away from the data receiver, test data may be permanently lost.

You may remove the data receiver from the docking station at any time during live monitoring without data loss if the data receiver is kept near the patient during the transition from being docked to being worn by the patient. When you remove the data receiver from the docking station, live monitoring stops.

The MotiliGI software cannot save test data displayed during live monitoring, but the data are stored on the data receiver and are downloaded as part of the completed test. 2. To exit live monitoring, click Stop on the live monitoring control panel. Appendix: Electrical Safety Aborting a Test Deactivating the Capsule Caution If a test is aborted before the capsule has been exposed to buffer solution, the capsule may be deactivated but must be used within two (2) hours or discarded. Caution If a test is aborted before ingestion and the capsule has not been exposed to buffer solution, the capsule may be deactivated but must be used within one month or before its expiration date is reached, whichever is sooner. Otherwise discard the capsule (refer to Recycling and Disposal Instructions, page 18). 1. Place the capsules container onto the activation fixture. 2. Align the diamond-shaped window on the capsules container with the Off mark on the activation fixture. 3. Leave the capsule container in place for 5 seconds and then lift straight up and off the activation fixture. 4. Confirm the capsule is deactivated:

Place the capsule container in the docking stations well and observe the data receivers display. The capsule is off if this icon an X. The X may take 1-2 minutes to appear.

(lower right) is replaced with Appendix: Electrical Safety

To determine capsule exit, you can observe the data display on the data receiver for at least 2 minutes. If the data receiver is receiving data from the capsule, this icon appears every 2040 seconds, which confirms that the capsule is still in the patient. No evidence of the icon within the 2-minute observation is presumptive evidence of capsule exit. Actual passage can only be confirmed clinically by examination of the graph or physical examination. Returning the Data Receiver Following the test, the patient returns the data receiver and patient diary to your office. A nurse or medical technician can perform these steps. 1. Collect the data receiver. 2. Ask the patient about his or her experience with the SmartPill test. Use MotiliGIs Post-Test Notes screen for recording information:

Did the patient experience any unusual cramping, pain or discomfort?

At any time during the test was the patient separated from the data receiver?

Did the patient observe the capsule in their stool confirming body exit?

3. Collect the patient diary. Review the diarys contents to ensure the patients notes are legible and comprehensible. 4. Release the patient. Downloading a Test 1. Turn on the data receiver. 2. Connect the docking station to a source of AC power and to the system computers USB port. Check the data receivers battery power. If battery power bars are not visible in the lower-

right corner of the data receiver, turn the data receiver off and charge it for 10 minutes before downloading. 3. Dock the data receiver in the docking station. 4. Launch the MotiliGI software and log in.

The software detects when the data receiver contains test data. A message asks whether you want to open the patients information. 5. Click Yes. The patients file opens. The file name appears in MotiliGIs title bar. 6. Download the data:

Appendix: Electrical Safety

Select Action > Download Data.

Click the The Patient Information screen opens. toolbar icon. Post Test Notes 7. In the Procedure Notes tab, click in the post-test notes field to enter notes elicited from the patient which were captured when the patient returned the data receiver.

See Adding and Creating a Template. 8. Click OK. (If you click Cancel, the data receiver continues to record capsule data and events.) The Test Download screen appears. Duration of test Duration of download (typical)

<3 minutes

<5 minutes 2 days 4 days MotiliGI protects current test data stored on the data receiver until current test data is completely downloaded. When the download is complete the MotiliGI software displays the entire test graph and the Test Summary screen. 9. Turn the data receiver off and place in the docking station to be recharged. Appendix: Electrical Safety Confirming Capsule Exit Caution Physicians should confirm capsule exit. Monitor patients until capsule passage is confirmed. 1. Use one of these methods:

Ask the patient whether the capsule was observed in his or her stool.

Download the test. Analyze the MotiliGI graph for evidence of exit: an abrupt drop in temperature or loss of signal that coincides with a diary entry for a bowel movement.

If you cannot confirm capsule exit cannot using these methods, or suspect a bowl obstruction, consider an abdominal x-ray and treat consistent with your management of a foreign object causing obstruction. An abdominal x-ray determines whether the capsule is retained and its location within the GI tract. If you suspect a delay in passage and the capsule is in the stomach, consider:

A pro-motility drug to help empty the capsule from the stomach.

Endoscopy to retrieve the capsule. If the capsule is in the colon, consider:

Laxative therapy to facilitate capsule movement.

Colonoscopy to retrieve the capsule. Appendix: Electrical Safety

The MotiliGI software identifies capsule ingestion, gastric emptying, ICJ, body exit, and computes GET, SBTT, CTT, SLBTT, WGTT, and motility indices. You can:

Match events with patient diary entries.

Analyze test to mark capsule ingestion, gastric emptying, ICJ and body exit.

Compare the markers you defined with markers identified by the MotiliGI software. Introduction to the Test Analysis Wizard After downloading a test, a message appears asking if you want to analyze the test. 1. Click Yes. The Test Analysis Wizard appears. You may close the wizard at any time. If you close the wizard before completing the analysis:

The Test Summary screen does not appear.

The test report will contain the note Test data not reviewed by physician.

The test wizard automatically saves. To re-open the wizard:

toolbar icon.

Click the

Select Action > Analyze Test. The test analysis wizard resumes from your last completed step. Appendix: Electrical Safety Figure 6 - Test Analysis Wizard Appendix: Electrical Safety 1 2 Navigates to any step of the wizard that you have completed Yellow light: You must take action to complete this step. Green light: You have completed this step. To take an action, click a link. You can enter notes. 3 4 Analyzing the Test Patient Diary Events The graph displays each event in succession. 1. Match each journal event with a recorded event, based on time, from the diary. a. Select an event icon, displayed in this step. b. c. Click Next Event to navigate through all events in the graph.

(Optional ) Enter a caption and notes.

To go back to an event click Previous Event.

If you cannot find a matching event in the diary:

Select None/No Match from the list. Appendix: Electrical Safety

Hide the event by uncheck the box Show the Event on the Graph. You can edit this information at any time by using the Point Annotation Viewer or the Annotation Viewer:

2. Click Next >. Select Capsule Ingestion Term Ingestion Definition The point where you observe the temperature beginning to rise to body temperature. Often, a pH spike to an off-scale value then a decrease to physiologic pH occurs just before ingestion due to exposure of the capsule to air.2 1. Click Mark ingestion on the graph 2 Fackler, WK, et. al. Ambulatory gastric pH monitoring: proper probe placement and normal values. Aliment Pharmacol Ther 2001; 15:1155-1162 2. Move the cursor over the graph and click on the location where you believe ingestion occurred. Appendix: Electrical Safety 3. Click Next >. Gastric Acidity A stomach baseline pH below 4 indicates normal acidic conditions. Baselines above 4 may indicate ineffective gastric acid production, buffering due to meals, or medications that suppress gastric acid. Click Next >. Procedure Deviation Additional Meal Before 6 Hours Appendix: Electrical Safety Snacks or meals may be recorded in the diary. A rise in pH and drop in temperature may indicate a meal response in the stomach. In figure above there is no evidence of an additional meal prior to capsule gastric emptying. See the figure below describing an ingested liquid meal Caution Eating anything (except limited quantities of water) before the capsule has emptied the stomach will delay gastric emptying and invalidate GET results. Click Next >. Food and liquid intake cause a rise in pH which can be mistaken as gastric emptying. Appendix: Electrical Safety Figure 7 - Eating a meal In the figure above, the patient ingested a liquid meal (Ensure) at 6 hours after capsule ingestion and ate dinner approximately 8 hours after capsule ingestion. The ingestion of food (Ensure and dinner) caused an abrupt rise in pH (B) and a decrease in temperature (A). At approximately 12 hours after capsule ingestion, the pH returned to baseline (below pH 2) and remained at baseline until the capsule emptied the stomach 18 hours after ingestion (C). Select Gastric Emptying Appendix: Electrical Safety Use GET to evaluate the patients gastric emptying function. Generally, an abrupt increase of 3 or more pH units occurs as the capsule exits the stomach and enters the duodenum. Term Definition Gastric emptying Sustained pH increase The beginning of the first increase in pH that results in a sustained pH rise. No transient pH drops occur for greater than 10 minutes. Caution Medications, therapies, and diseases may alter gastric or small bowel pH. Alterations in gastric and/or small bowel pH may mask the physiological pH landmark for gastric emptying time. 1. Click Mark gastric emptying on the graph. 2. Move cursor over to the MotiliGI graph and click on the graph where you believe gastric emptying occurred. 3. Click Next >. Magnitude of pH Rise at Emptying Appendix: Electrical Safety Definition Determined by observing the pH within the first 30 minutes after gastric emptying. No transient pH drops occur for greater than 10 minutes. Term Duodenal pH baseline Sustained pH increase Click Next >. Gastric Pressure Characteristics Appendix: Electrical Safety The relevance of SmartPill pressure patterns in the stomach to pressure patterns obtained using manometry is unknown. Click Next >. Small Bowel pH profile 1. Determine whether you observe a gradually rising pH profile characteristic of the small bowel. Appendix: Electrical Safety 2. Click Next >. Small Bowel Pressure Characteristics The clinical significance of SmartPill pressure patterns in the small bowel is unknown. Click Next >. Select Ileo-Cecal Junction Appendix: Electrical Safety The standard small bowel pH profile shows a gradual pH rise usually followed by a plateau of the pH pattern. Transient pH drops may interrupt this profile but returns to their previous level within 10 minutes. The pH drop associated with the capsule passing through the ICJ occurs after the gradual sustained increase in pH through the small bowel. This drop of approximately 0.51.0 pH units usually occurs between 26 hours after gastric emptying. 3 Before ICJ, the pH rises smoothly and continuously in comparison to a more erratic profile after ICJ. Term ICJ Click Next >. Definition Ileo-Cecal Junction, the start of pH decrease of approximately 0.51.0 units. 3 Zarate N., Scott SM. Accurate localisation of a fall in pH within the ileo-caecal region: validation using a dual scintigraphic technique. Am J Physiol Gastrointest Liver Physiol 2010; 299 (6): G1276-86. Colonic Pressure Characteristics Appendix: Electrical Safety The relevance of SmartPill pressure patterns in the colon to colonic pressure patterns obtained using manometry is unknown. Click Next >. Appendix: Electrical Safety Warning: Data Collected During Capsule Low Voltage If the MotiliGI software detects a low voltage condition in the capsule, a warning appears. Caution When a low voltage warning is present, body exit confirmation cannot be determined solely by temperature drop. Low voltage may cause loss of signal before capsule exits the body. Whole gut and small/large bowel transit times are not definitive without the body exit endpoint. Regional transit times are not valid without start and endpoints. 1. Read and understand the warning. 2. To acknowledge this warning, check the box I Understand. 3. Click Next >. Select Body Exit Appendix: Electrical Safety Term Body exit Definition

The time of the last temperature reading at body temperature, coinciding with an abrupt loss of capsule data.

The time of the last abrupt rise in pressure. An abrupt loss of signal from the capsule does not reliably indicate body exit. You must corroborate (to within 30 minutes) body exit with a recorded bowel movement in the patient diary. Appendix: Electrical Safety Figure 8 - Body Exit The figure above provides an optimal representation of body exit including a bowel movement event marker on the graph and in the patient diary temperature drop (A), a decrease in temperature (B) and an abrupt loss of data (C). Caution If the diary does not contain a bowel movement entry concomitant with a temperature drop and/or loss of pressure and pH signal, the patient should be monitored for symptoms of bowel obstruction. If the patient exhibits symptoms consistent with bowel obstruction, a KUB exam is indicated. Click Next >. Review Your Physiological Markers with MotiliGI Appendix: Electrical Safety Description Dashed vertical line on the graph, labeled computed. Solid vertical lines. Your marker and the computed marker are within 5 minutes of each other, labeled equivalent. The computed time is grayed out. Term Computed markers Your markers Equivalent Click Next >. MotiliGI-Computed Capsule Ingestion Appendix: Electrical Safety MotiliGI determines ingestion by finding the point at which temperature stabilized at body temperature. 1. Follow the prompts. 2. Click Next >. MotiliGI-Computed Gastric Emptying Appendix: Electrical Safety MotiliGI selects gastric emptying by finding the beginning of the abrupt, sustained pH rise. Medications, therapies, and diseases that alter gastric or small bowel pH may influence the accuracy of computed gastric emptying. 1. Follow the prompts. 2. Click Next >. Absence of Gastric Emptying If you did not identify gastric emptying, the wizard reminds you of the omission and asks you to select gastric emptying. Appendix: Electrical Safety

To review the MotiliGI computed gastric emptying, click <Back. Caution If gastric emptying is not observed, body exit should be confirmed by analysis of data. If body exit cannot be confirmed, the patient should be monitored for symptoms of bowel obstruction. If the patient exhibits symptoms consistent with bowel obstruction, a KUB exam is indicated to determine capsule exit or retention. 1. Follow the prompts and select Yes or No. 2. Click Next >. Gastric Emptying Statistics Appendix: Electrical Safety This step allows you to enter observations about the gastric emptying statistics. Click Next >. Gastric Emptying Time Evaluation Appendix: Electrical Safety Use GET to evaluate the patients gastric emptying function. Term Premature gastric emptying Normal gastric emptying Delayed gastric emptying Click Next >. Definition Within 30 minutes of ingestion. After 2 hours but before 4 hours of ingestion. After 4 hours of ingestion. MotiliGI-Computed ICJ Appendix: Electrical Safety MotiliGI selects ICJ by looking for the first and largest pH drop between 30 minutes and 6 hours after gastric emptying. 1. Follow the prompts. 2. Click Next >. Small Bowel Transit Time Evaluation Appendix: Electrical Safety The clinical significance of SmartPills transit time in the small bowel is unknown. Click Next >. MotiliGI-Computed Body Exit Appendix: Electrical Safety MotiliGI selects body exit based on temperature and pressure. An abrupt loss of signal from the capsule does not reliably indicate body exit. You must corroborate (to within 30 minutes) body exit with a recorded bowel movement in the patient diary. Caution If the diary does not contain a bowel movement entry concomitant with a temperature drop and/or loss of pressure\pH signal, the patient should be monitored for symptoms of bowel obstruction. If the patient exhibits symptoms consistent with bowel obstruction, a KUB exam is indicated. 1. Follow the prompts. 2. Click Next >. Absence of Body Exit If you did not identify body exit, this step appears. Appendix: Electrical Safety

To review the computed body exit, click <Back. Caution If the diary does not contain a bowel movement entry concomitant with a temperature drop and/or loss of pressure and pH signal, the patient should be monitored for symptoms of bowel obstruction. If the patient exhibits symptoms consistent with bowel obstruction, a KUB exam is indicated. Caution If MotiliGI displays a low voltage indication on the graph, the validity of data collected during the low voltage state cannot be determined, including any temperature drops that mimic body exit. 1. Select Yes or No. 2. Click Next >. Colonic Transit Time Evaluation Appendix: Electrical Safety MotiliGI uses your interpretation of ICJ (colonic entry) and body exit events to compute the CTT. Click Next >. Test Analysis Review The analysis is complete. Appendix: Electrical Safety Click Finish. Reading Test Summary Reports When the test analysis wizard is complete, a summary report of results and descriptive data appears. These reports summarize test data, statistics, and observations, and help evaluate delayed gastric emptying, constipation and gastrointestinal motility. You can display the test summary reports any time:

Click the

Select View > Test Summary. toolbar icon. Transit Data Tab This tab lets you compare your transit time data to the computed data. Appendix: Electrical Safety

If one or more endpoint markers are not defined, n/a (not applicable) appears for the transit time value.

Combined small and large bowel transit time (SLBTT) can be used as a surrogate measure for CTT when CTT cannot be determined. You can edit the data at any time, and the corresponding reports update accordingly:

Action Tools to use For more information Edit ingestion time, gastric emptying time and body exit time Graph marker tools Chapter 8: MotiliGI Features Edit or enter motility statistics Statistics Mode tools Chapter 8: MotiliGI Features Descriptive Data Tab This tab summarizes calculated pressure and pH data points. The clinical significance of these pressure and pH descriptive statistics is unknown. Appendix: Electrical Safety Appendix: Electrical Safety Interpretations Tab This tab displays notes made during analysis and provides a text section for capturing post-test observations, conclusions and recommendations. The information entered in this tab becomes part of the patients record. Alternatively, you can enter interpretations through the Interpretations tab of the Patient Information screen. Interpretations can be entered before or after the test is downloaded. Click to use preconfigured templates to describe test interpretations. Goal Create a template Delete a template Add the description to the patients record Remove the description from the patients record Print a description in the final report Action Enter a title in the Template field and a description in the text field below it. Click Save Template. Select the title in the Template list. Click Delete Template. Select the template title. Click Select the description in the Patient record box. Click Remove Entry. Select checkboxes in the Patient record box. Properties Tab This tab displays information about the equipment used for the test. Appendix: Electrical Safety Examples of Physiological Markers Ingestion The ingestion landmark starts the test and is the beginning of GET. MotiliGI determines the ingestion landmark by finding the point just before temperature stabilizes to body temperature, as illustrated below. The pH also starts to become more acidic. Appendix: Electrical Safety A B Figure 9 - Ingestion Gastric Emptying Gastric emptying marks the end of GET and the start of SBTT as shown below. Figure 10 - Gastric Emptying MotiliGI looks for an abrupt increase of 3 or more pH unit as the capsule exits the stomach and enters the duodenum. Appendix: Electrical Safety Factors that may influence gastric emptying include:

Medications, therapies, and diseases that alter gastric or small bowel pH. ICJ ICJ is usually found between 2 to 6 hours after gastric emptying, as seen below. ICJ marks the transition of the capsule from the small bowel into the colon. ICJ marks the end of SBTT and the start of CTT. How to find ICJ:

1. Locate gastric emptying 2. Look for a steady rise in pH followed by a plateau. 3. Look for a 1 to 2 unit pH drop between 2 to 6 hours after gastric emptying

A high amplitude spike in pressure is often seen near ICJ

After ICJ an erratic pH profile in the colon is characteristic C ICJ E D A B Figure 11 - ICJ Body Exit Time Body exit marks the end of the test as shown below. Body exit marks the exit of the capsule from the body and the end of WGTT and CTT. Appendix: Electrical Safety Figure 12 - Body Exit Appendix: Electrical Safety

MotiliGI User Interface The MotiliGI user interface consists of main dropdown menus, toolbar, graph area, control panels, time slider control and status bar. Figure 13 - MotiliGI User Interface Titlebar Labeled A on Figure 13. The titlebar displays the filename constructed from the Patient ID and the time and date of the beginning of the test, for example Patient ID #207516, 9:29:44 AM, 28 March, 2007. Main Menus Labeled B on Figure 13. Toolbar Icons Labeled C on Figure 13. Back to Previous View Forward to Next View New Start a new test Appendix: Electrical Safety Open Open a test. You can choose to open by patient name or filename. Live Monitoring Download Data Analyze Test Print Print Preview Generate Report Test Summary Patient Info Annotation Viewer Display Ingestion Display Stomach Display Gastric Emptying Display Small/Large Bowel Display Body Exit Display Entire Test Show/Hide Pressure Show/Hide pH Show/Hide Temperature Zoom In Zoom Out Show/Hide Annotations Annotations Statistics Set Ingestion Marker Appendix: Electrical Safety Set Gastric Emptying Marker Set ICJ Marker Set Body Exit Marker Graph Area Labeled D on Figure 13. The graph area presents plots of pressure, pH, and temperature data captured throughout the test, and point and range annotations. The left Y-axis is the pressure scale, the right Y-axes are pH and temperature scales, and the X-axis is the elapsed time of the test. Data Panels Labeled E on Figure 13. MotiliGIs two data panels, positioned to the right of the graph area, provide information and controls related to test Statistics and graph Location. To show or hide the data panel:

Double-clicking the bar between the graph and the data panels. Time Slider Control Labeled F on Figure 13. The time slider control shows what appears in the main graph in relation to the entire test. Display Tabs Labeled G on Figure 13. Navigate between the Graph (statistics panel), Help (user manual) and Analysis Wizard

(not pictured). To show or hide the data panel:

Double-clicking the bar between the graph and the data panels. Status Bar Labeled H on Figure 13. The status bar displays the username, and data receiver and test status icons. MotiliGI uses 7 icons to indicate the status of the data receiver and test. Appendix: Electrical Safety Data Receiver Status Icons Icon Description Disconnected No USB connection exists between MotiliGI and the data receiver. Connected MotiliGI is communicating with the data receiver. Test Status Icons Icon Description Capsule Not Found MotiliGI is not receiving data from a capsule and indicates a capsule has not been activated or the capsule is out of range of the data receiver. Test Status Unknown MotiliGI cannot determine the status of the test. Test Ready to Begin MotiliGI is properly communicating with the data receiver and the capsule. This icon appears during capsule calibration. Test in Progress The test has begun. The data receiver is recording data from the capsule. Test Ended Data collection has stopped. This icon appears during data download. MotiliGI Keyboard Shortcuts Keyboard Shortcut Effect Control X Control C Control V Tab Enter Cut text from any form field, copied to the clipboard Copy text from any form field to the clipboard Paste text from the clipboard to any form field Move from one text field to the next Press the default button for the current form, panel, or dialog box

1. Open a test:

on the toolbar.

Click

Click File > Open 2. Select By Patient Name. The Find Patient window appears. Appendix: Electrical Safety

To show all tests in the Results box, click Show All Tests.

To reduce the size of the list, enter all or part of the patients name or patient ID. You can also enter a test date or range of dates in the Find by test date box. 3. Click Search. MotiliGI displays matching tests in the Results box. 4. Click a row to select the patients test. 5. Click Open. Opening a Test by the File Name 1. Open a test:

on the toolbar.

Click

Click File > Open 2. Select By Filename. The Open File screen appears. 3. Browse to the test file:

Windows XP: C:\Documents and Settings\All Users\Application Data\SmartPill\Tests

Windows 7: C:\ Program Data\SmartPill\Tests 4. Click Open. Closing a Test Select File > Close. MotiliGI saves changes to the test when you close. Appendix: Electrical Safety Exiting MotiliGI MotiliGI saves changes to the test when you exit. To exit MotiliGI, either:

Select File > Exit

Close using the Caution Do not close MotiliGI while operating the Test Initiation Wizard because data can be lost. Complete or abort the Wizard first. in the upper right hand corner. Caution Do not close MotiliGI while downloading a test because data can be lost. Allow the test to fully download. Setting General User Preferences Each user can have saved preferences for the General, Graph and File tabs. Report preferences apply to all users. To customize the look and feel of the user interface:

Select Tools > Options. General Tab You can select preferences for the User Interface:

The number of tests appearing in the File > Recent Tests menu. Appendix: Electrical Safety

The number of physicians names appearing in the Ordering and Primary Care Physician drop down lists on the General tab of the Enter Patient Information screen.

The display language. Changes will take effect when you restart MotiliGI.

The unit of measure, English or metric. You can select preferences for the view displayed when MotiliGI opens a test:

Ingestion and the number of hours displayed after ingestion

Stomach

Gastric emptying and the number of hours displayed before and after gastric emptying

Small/large bowel

Body exit and the number of hours displayed before body exit

Entire test Graph Tab You can select preferences for the Plot Area Properties for Time, Pressure, pH and Temperature:

Color, line style, and point style of data plot Appendix: Electrical Safety

Show or hide the plot

The ranges, tick values and colors of the X and Y axes You can select preferences for Visibility:

Show or hide gridlines, annotations, and missing data packets You can select preferences for Color Scheme:

The color of gridlines, annotations, title text, and background color Report Tab You can select an option for printing reports. MotiliGI lets you print reports on your own letterhead stationery or create a custom letterhead. You can select report options. You can choose to include the following in the report:

Letterhead and paper size

Administrative information including test statistics, study comments, and screen prints of the Test Summary screens.

The patients information.

The Annotation information including statistics and notes.

The plots to be graphed: pressure, pH, temperature and annotations.

The graph views of the test. Appendix: Electrical Safety Creating Report Letterhead 1. Select Tools > Options > Report Tab. 2. Choose paper size. 3. Click Create Letterhead.

The Letterhead Creator appears:

Add text to the letterhead 1. Click New Text Box. A text box appears in the new letterhead. 2. Type the desired text. 3. Click and drag the text box to move to a location in the Letterhead Canvas.

You can modify the font, resize the text box or delete the text box. a. Right-click in the text box. b. Choose desired option. c. To resize the text box drag your mouse to the desired size and click to apply. d. Click OK. 4. Click Save. Add an image to the letterhead 1. Click New Image Box. An image box appears in the new letterhead. 2. Right-click in the image box to select an image. 3. Click Browse for Image... An Open Image screen appears. 4. Find and select a bitmap, JPEG or GIF file. 5. Click OK.

You can modify the image appearance, resize or delete the image box. Right-click in the image box. Choose desired option. Appendix: Electrical Safety

To resize the image box drag your mouse to the desired size and click to apply. 6. Click Save. Files Tab You can select the target folder to save files to.

Click Browse to find target folder.

Type in the folder location. Setting Preferences Back to Default Click Restore Defaults to return all tabs and settings to default states. Your language preference remains the same. Editing Patient Information Edit patient information any time after the start of the test. Patient information is initially entered in the test initiation wizard. You can edit information on all tabs within the patient information screen. If you edit the patient ID, MotiliGI updates the electronic test filename, log filename and the folder containing the files with the new patient ID number and it will ask you to confirm. If you previously generated a report (WordPad document), your report filename and patient ID number will not be updated. You will need to generate a new report. 1. To access the patient information either:

on the toolbar

Click

Click View > Patient Info. Appendix: Electrical Safety 2. Edit the patients information. 3. Click OK. Changing the Graph Display Selecting Data Plots MotiliGI gives you 3 methods to select the data (pressure, pH and temperature) displayed on the graph:

Method 1 Context Menu

Right-click on the graph and select a data plot. A checkmark indicates the plot appears on the graph. Appendix: Electrical Safety Method 2 Toolbar Icons Click on a Show/Hide data plot icon. Show/Hide Pressure Show/Hide pH Show/Hide Temperature toolbar icon. toolbar icon. Method 3 Main Menu Click View > Plots. Select a data plot icon to toggle the plot. Changing the Test View

To undo any view operation, click the

To redo a view operation, click the MotiliGI prefers the physician-determined marker rather than the computed marker to define the regions. MotiliGI gives you several methods to select a test view. Method 1 Context Menu Right-click on the graph and select a desired view. Method 2 Main Menu Click Go and choose a desired view. Method 3 Toolbar Icons Click on a display icon Display Ingestion Test data around the ingestion marker. Appendix: Electrical Safety Display Stomach Test data between the ingestion marker and the gastric emptying marker. Display Gastric Emptying Test data around the gastric emptying marker Display Small/Large Bowel Test data from the gastric emptying marker to the body exit marker. Display Body Exit Test data around the body exit marker. Display Entire Test Test data from the ingestion marker to the body exit marker. Method 4 Time Slider Control The portion of the test shown in the graph area is highlighted in white. To move the slider:

1. Place your cursor on the slider. The cursor changes to a finger. 2. Click and drag the cursor to the left or right. 3. Release the cursor. The main graph updates.

You can also move the slider with the scroll wheel on the mouse. To zoom with the slider:

1. Place your cursor over the border of the highlighted area. The cursor changes to a double arrowhead. 2. Click and drag the border to the left or right. 3. Release the cursor. The main graph updates. Method 5 Zoom Controls To zoom in:

1. From the toolbar, select 2. Select an area to view by:

. The cursor changes to a magnifying glass icon.

Clicking on a graph location (This method only zooms in on the X axis) Appendix: Electrical Safety

Clicking and dragging your mouse to select a graph region (This method zooms in on both the X and Y axis) 3. Click to exit the zoom in mode. The cursor returns to normal.

To return to your last view use the icon. To zoom out:

1. From the toolbar, select 2. Select an area to view by clicking on a graph location. 3. Click Method 6 Using the Data Panel: Location to exit zoom out mode. The cursor returns to normal. The cursor changes to a magnifying glass icon. 1. Define a window of time by selecting Start and End Times or Time In Center 2. Enter the time you wish to display. 3. Click Set Graph. Changing Axis Scales Y Axes To change the scale of the pressure, pH or temperature axis:

1. Double-click on the desired axis. 2. Enter the new axis scale minimum and maximum values. 3. Click OK. To restore the scale to the saved user preferences:

1. Double-click on the desired axis. 2. Click Restore Axis Defaults or Restore Defaults for All Axes. Appendix: Electrical Safety 3. Click OK. X Axis To change the time format between calendar date/time and elapsed time either:

Double-click on the time axis to toggle between elapsed time or real date/time.

Go to Tools > Options >Graph > Time Axis Analyzing Data Showing and Hiding Annotations Annotations include patient diary events, range annotations, and point annotations. Annotations are visible by default.

To toggle the visibility of all graph annotations, click Editing Patient Diary Events To view and edit patient diary events 1. Open the Annotation Viewer:

Click

Select View > Annotation Viewer. The Annotation Viewer screen appears. on the toolbar. on the toolbar. 2. Click the event you wish to edit. The event details appear in the annotation properties box. 3. Select an icon from the Journal Event drop-down list. The Update button appears. Appendix: Electrical Safety

(Optional) You can enter text in the Caption box and in the Notes box. Caption text shows on the graph, while Notes text shows in the Annotation Viewer and in the printed report.

You can click the checkboxes to show or hide the annotation and the caption. 4. Click Update to save changes. Disregard diary entries and events that do not have a reasonable time correlation. Creating New Event Annotations To enter an event that does not appear on the graph:

1. Click 2. Click on the graph at the appropriate time to create the annotation. The Point on the toolbar. The cursor changes to a similar icon. Annotation Editor appears. 3. Select an icon from the Icon dropdown box.

(Optional) You can enter text in the Caption box and the Notes box. Caption text shows on the graph. Notes only show in the Annotation Viewer, Point Annotation Editor and in the printed report.

You can view the time, pH and pressure values at the selected graph point.

You can click the checkboxes to show or hide the annotation and the caption. 4. Click OK. on the toolbar. The cursor returns to normal. To exit the Annotation mode, click Editing Event Annotations Event icons cannot be moved, only deleted or hidden. An event created by the patient pushing the event button on the data receiver cannot be deleted; it can only be hidden. Physician-created annotations can be deleted.

Double-click the event icon. The Point Annotation Editor appears. Appendix: Electrical Safety on the toolbar.

1. Click 2. Move cursor over the caption text. The cursor changes to a crosshair. 3. Click and drag the caption text to a new location. To delete an annotation:

1. Double-click the event icon. The Point Annotation Editor appears. 2. Click Delete. Adding or Changing the Location of Physiological Markers Physiological markers are used to compute transit times. MotiliGI-computed markers appear on the graph as dotted vertical lines. Physician-defined markers appear on the graph as solid vertical lines. Physiological Markers Ingestion - Time the capsule was ingested Gastric emptying - Time the capsule left the stomach Ileo-cecal junction - Time the capsule entered the colon Body exit - Time the capsule left the body Marker Color Blue Silver Green Magenta Toolbar Icon To add or change the location of a marker:

1. Click the appropriate toolbar icon. The cursor changes to a crosshair. 2. Click the graph to set the marker at a location. The cursor returns to normal. To clear (delete) a physician-defined marker:

Select Markers > Clear Defined Markers You can choose to clear one or all physician-defined markers. To hide a marker:

Select Markers > Show/Hide Markers You can choose to show/hide one or all physician-defined and MotiliGI-computed markers. Appendix: Electrical Safety Viewing Transit Times

Click on the toolbar.

Select View > Test Summary The Test Summary screen appears. Transit times computed using the physician-

defined markers appear on the left and MotiliGI-computed markers appear on the right. Calculating Statistics To enter the Statistics mode:

on the toolbar. The cursor changes to 1. Click 2. Click and drag to select any area of the graph. A yellow box appears around the selected area and creates a range. The Statistics panel displays pressure, pH and temperature statistics for the range. To save the range as an annotation on the graph:

1. On the statistics panel, click Save Annotation. The Range Annotation Editor screen appears.

(Optional) You can enter text in the Caption and Notes boxes.

You can click the checkboxes to show or hide the annotation and the caption. 2. Click OK. Appendix: Electrical Safety You can create and save multiple range annotations. on the toolbar. The cursor returns to normal. on the toolbar. The cursor changes to To exit the Statistics mode, Click To edit a range annotation:

1. Click 2. Double-click the border of a range. The Range Annotation Editor screen appears. 3. Edit the annotation. 4. Click OK. To view the statistics of a range annotation:

Hold the cursor over the yellow border of the range. The statistics appear in the Data Panel - Statistics. Creating Output Generating a Report 1. You can either:

Click on the toolbar, or Appendix: Electrical Safety

Select Action > Generate Report The report opens in Microsoft WordPad. MotiliGI immediately saves the report to the patients folder using a default name. Caution Edits made to the WordPad report will not be saved to the MotiliGI test. To save the report:

1. Select File > Save As. 2. Type in a new name in File Name. 3. Click Save. Saving the Report as a PDF File 1. In WordPad, select File > Print. The Windows Print screen appears. 2. In the Printer Name drop down menu, Select PDFill PDF Editor. 3. Click Print. The Save PDF File As screen appears. 4. Enter a filename 5. Click OK. Printing the Graph You can use Print Preview to check the graph before you print it. To preview, either

Select File > Print Preview, or

Click on the toolbar. To print the graph, either:

Select File > Print

Click on the toolbar. The Windows Print screen appears. Follow the on-

screen instructions. Exporting Data to Excel You can export test data (pH, pressure and temperature) to a text file in comma-

separated value format. You can export data from the current graph view or from the entire test. To Export the Current Graph View 1. Select File > Export > Test Data Snapshot. A Save As screen appears.

MotiliGI creates a folder that contains separate CSV files for pH, pressure and temperature. Appendix: Electrical Safety 2. Name the folder. 3. Click Save. To Export the Entire Test 1. Select File > Export > Complete Test Data. A Save As screen appears

MotiliGI creates a folder that contains separate CSV files for pH, pressure and temperature. 2. Name the folder. 3. Click Save. To Export Individual Data Sets 1. Select File > Export > Customize Export. The Export Options screen appears. 2. Select the desired preferences.

You can select to export data sets from the complete test or current view.

Check Trim After BET if you do not want to export data after body exit.

Check Wrap Columns for Microsoft Excel. This feature wraps data sets larger than 32000 rows into adjacent columns.

Under Data Export Options, select one or more data sets to export.

Under each data set, select one or more parameters to export.

Check Export Test Summary to export the transit and descriptive data from the Test Summary Screen. 3. Click Export. Data Parameter Definitions

Timestamps are in milliseconds starting at capsule calibration.

Raw Data is in millivolts.

Converted Data is raw data multiplied by the sensors scale factor. Appendix: Electrical Safety Data Set pH Pressure Temperature Units pH units mmHg C

Calibrated Data is converted data adjusted by the calibration point (pH 6, atmospheric pressure, room temperature).

Temperature Compensated is the calibrated data adjusted for sensor drift due to increased temperature.

Baseline Compensated is temperature compensated data with the baseline adjusted to 0. Exporting Images to JPEG or GIF You can export graphs to an image file in JPEG or GIF format. You can export images from the current graph view or from the entire test. To export the image of the current graph view:

1. Select File > Export> Graph Image Snapshot. A Save As screen appears. 2. Name the file. 3. Select file type from the dropdown box. 4. Click Save. To export the image of the entire test:

1. Select File > Export> Complete Graph Image. A Save As screen appears. 2. Name the file. 3. Select file type from the dropdown box. 4. Click Save. Appendix: Electrical Safety

Password Management Logging into the System Computer For security purposes, after 5 unsuccessful attempts to logon, the user will not be allowed to logon for 15 minutes Enter the Windows user name and password noted below. User Name Password Privileges sgims1 12345 Administrator Password supplied by Technical Support Can operate the computer and save documents. Can install programs, printers or change system settings by using MotiliGI Administrator.

To change the user name or password, contact Technical Support for assistance. Used in emergency situations. Can install programs, printers or change system settings. Windows Administrative Logon (IT Administrator use only) Under normal circumstances, use of this account should not be necessary. To log in as the Windows administrator:

1. Turn on the SmartPill System Computer 2. Log into the Windows sgims1 account (see system computer above). 3. Go to the Windows Start Menu > SmartPill> MotiliGI Administrator. 4. Enter the MotiliGI Administrator password and click Login. 5. Click Retrieve Key 6. Upon retrieving the key, contact Technical Support to obtain an administrative password that can only be used once. After obtaining the password:

7. Go to Start>Log Off 8. Log into Windows. Enter Administrator into the username field and the password provided by SmartPill into the password field. Appendix: Electrical Safety Logging into MotiliGI When using MotiliGI for the first time, an administrator account is set up. The administrator has privileges to set up additional users and, edit user names and passwords. Forgotten Password If a user has forgotten his or her password, the administrator must log into MotiliGI and reset the users password. If the administrator has forgotten his or her username or password, they must call Technical Support.

The Reset Password option resets the selected users password to 12345. MotiliGI Security Security Tab You must be logged into MotiliGI as the administrator to view the security tab. To log in as the administrator:

1. Go to Tools > Login In As 2. Type in the administrator username and password. 3. Click Log In. To change the security settings:

Go to Tools > Options > Security Appendix: Electrical Safety Security enabled is the default setting and requires users to log in with their username and password. Security disabled eliminates the login (user authentication) step. The user will be logged into the default user account. Recommendation: Assign a unique username and password to each MotiliGI user. The username is used as the Technician Name in the printed report. Adding a User 1. Go to Tools > Options > Security. 2. Under User Management click Add. 3. Under Add User, enter a user name and password (both require a minimum of 5 alpha-numeric characters). 4. Click OK. The new user will appear in the Current Users box. Removing a User Select the username from the list of current users and click Remove. To change a username, select the user from the list of current users, click Remove and then add a new user. Backing Up Patient Files 1. Verify that MotiliGI is closed (not running). 2. Insert a blank CD into the CD Drive or insert a USB drive into a USB port. 3. Double-click on the Tests icon on the Desktop. 4. Right-click on the patient record folder, click Send To > Compressed (zipped) Folder. 5. Right-click on the Patient_xxxx.zip file you just created, where xxxx is the patients ID. Click Send To > DVD/CD-RW Drive (D:) or Removable Disk (E:). on the toolbar. 6. Click 7. Right-click on the Log folder, click Send To > Compressed (zipped) Folder. 8. Right-click on the Log.zip file you just created and click Send To > DVD/CD-RW Drive (D:) or Removable Disk (E:). If you are writing to a CD:

a. Click on the balloon You have files waiting to be written to the CD. b. Under the CD Writing Tasks heading, click Write these files to CD. c. Confirm that the files have been written to the CD by opening the DVD/CD-RW Drive (D:) in Windows Explorer. If you are writing to a USB drive:

Appendix: Electrical Safety a. Confirm the files have been saved by opening the Removable Disk (E:) in Windows Explorer. b. Click

(E:). located on the right side of the Start bar. Select Safely remove the Removable Disk Installing Software To install third-party software, log into the system computer as the system computer administrator or utilize SmartPills MotiliGI Administrator application. Caution Exercise caution installing third-party software (e.g. applications, drivers) on the system computer. Installing third-party software not listed below may increase the potential for software conflicts with MotiliGI. SmartPill Approved Third-Party Software Microsoft Excel Microsoft Word Adobe Acrobat Reader PDFill PDF Editor Printer drivers Windows Accessories MotiliGI Administrator MotiliGI Administrator serves two purposes:

It provides the means to install a limited set of software.

It provides access to the administrative account. Launching MotiliGI Administrator 1. Turn on the system computer 2. Log into the system computer using the sgims1 account. 3. Go to the Start Menu > SmartPill> MotiliGI Administrator 4. Create a password. The password is case sensitive, must be at least five characters long, and must be confirmed. The MotiliGI Administrator password is independent of MotiliGI and must be entered for each subsequent running of MotiliGI Administrator. 5. Retype the password and click Login. Figure 14 After logging in, the MotiliGI Administrator screen will appear. Appendix: Electrical Safety Figure 15 Installing Software from a CD 1. Place the CD in the CD-ROM drive and click Update from CD. The contents of the CD will be displayed in the center box of the main screen. 2. Double click on the file you wish to install. Installing Software from a File on the System Computer Hard Drive 1. Locate the file you wish to install. 2. Move the file into C:\Program Files\SmartPill\ MotiliGI Administrator\Update\ Directory 3. Click Update from Folder. The contents of the update directory will be displayed in the center box of the screen. Figure 16 4. Double click on the file you wish to install. Appendix: Electrical Safety Uninstalling MotiliGI Caution If you find it necessary to uninstall MotiliGI, ensure you have backed up and/or saved patient test files, exported data files and reports (except those that have been saved as PDFs) to another location on your hard drive or to external media (e.g., auxiliary or external hard drive, CD). You must be logged into the system computer as the Windows administrator to uninstall MotiliGI. 1. Backup any data files you have created. 2. Close MotiliGI. 3. Log into the computer as the Windows administrator. 4. Go to the Windows Start Menu > Control Panel > Add/Remove Programs. 5. Locate and select MotiliGI in the programs list, click Add/Remove. 6. Select Yes to confirm removal of MotiliGI. 7. Delete the folder C:\Program Files\SmartPill\ MotiliGI Administrator\Update\ Directory Installing MotiliGI Use MotiliGI Administrator to reinstall or upgrade MotiliGI from a CD. 1. Reboot the system computer and log into the sgims1 Windows account. You must reboot the computer immediately prior to upgrading MotiliGI to avoid any problems. 2. Go to Start > All Programs > SmartPill folder > MotiliGI Administrator. 3. Enter the password and click Login. 4. Insert the MotiliGI CD into the CD-ROM drive. 5. Click Update from CD. Appendix: Electrical Safety Figure 17 6. Double-click on the MotiliGI folder. 7. Double-click on Setup.exe. Follow all instructions in the installation wizard. 8. When the wizard finishes, close the wizard and close MotiliGI Administrator. 9. Reboot the PC. If you are installing MotiliGI on a computer other than your system computer (for reading test data only), you will need to install Adobe Acrobat Reader 7.0 or greater for MotiliGI to run properly. MotiliGI is only compatible with Windows XP and Windows 7 32-bit operating systems. MotiliGI is not warranted for use with any other operating system. MotiliGI relies on the Microsoft .NET framework version 1.1. If you are installing MotiliGI on another computer to view test files, run the Windows Update feature of the Microsoft website (http://update.microsoft.com/windowsupdate) to check for and install any critical updates to the Microsoft .NET framework before completing the installation. The first time the data receiver is connected to the system computer, Windows XP will acknowledge it has found a new USB device and will load the drivers necessary for it to communicate with the data receiver. You may see a dialog box pop up asking for the Windows Administrator username and password. Do not take action MotiliGI administrator will automatically fill in the required information after a few seconds and the installation will continue. Appendix: Electrical Safety

External equipment intended for connection to signal input, signal output or other connectors shall comply with relevant IEC standard (e.g. IEC 60950 for IT equipment and the IEC 60601 series for medical electrical equipment). In addition, all such combinations systems shall comply with the standard IEC 60601-1-1, Safety requirements for medical electrical systems. Equipment not complying with IEC 60601-1 shall be kept outside the patient environment, as defined in the standard.4Any person who connects external equipment to signal input, signal output or other connectors has formed a system and is therefore responsible for the system to comply with the requirements of IEC 60601-1-1. If in doubt, contact a qualified biomedical engineer or Given Imaging. The following tables outline the SmartPill GI Monitoring Systems compliance with INTERNATIONAL STANDARD, International Electrotechnical Commission (IEC) IEC 60601-1-2, Medical electrical equipment Part 1-2: General requirements for safety Collateral standard: Electromagnetic compatibility Requirements and tests.

electromagnetic emissions The SmartPill GI Monitoring System is intended for use in the electromagnetic environment specified below. The customer or the user of the SmartPill GI Monitoring System assures that it is used in such an environment. Emissions test Compliance Electromagnetic environment guidance The SmartPill GI Monitoring System uses RF energy exclusively for its internal function. Thus the RF emission is very low and it is unlikely that nearby electronic devices would be disturbed. The SmartPill GI Monitoring System is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes. RF emissions CISPR 11 Group 1 Class B Complies IEC 61000-3-2 RF emissions CISPR 11 Harmonic emissions IEC 61000-3-2 Voltage fluctuations/flicker emissions IEC 61000-3-3 4 The normal distance is at least 1.5 m from the patient or the patient support.

electromagnetic immunity The SmartPill GI Monitoring System is intended for use in the electromagnetic environment specified below. The customer or the user of the SmartPill GI Monitoring System should assure that it is used in such an environment. Immunity test Compliance level Electromagnetic environment guidance IEC 60601 test level 6 kV contact 8 kV air 2 kV on AC mains 1 kV on measurement I/O lines 1 kV on Line to Neutral 2 kV on Line or Neutral to protected earth N/A Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%. Mains power quality should be that of a typical commercial or hospital environment. Mains power quality should be that of a typical commercial or hospital environment. N/A Electrostatic discharge (ESD) IEC 61000-4-2 6 kV contact 8 kV air Electrical fast transient/burst IEC 61000-4-4 2 kV for power supply lines 1 kV for input/output lines Surge IEC 61000-4-5 1 kV line(s) to line(s) 2 kV line(s) to earth Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11

<5 % UT (>95 % dip in UT) for 0.5 cycle 40 % UT (60 % dip in UT) for 5 cycles 70 % UT (30 % dip in UT) for 25 cycles

<5 % UT (>95 % dip in UT) for 5 sec 3 A/m Power frequency

(50/60 Hz) magnetic field IEC 61000-4-8 Note UT is the a.c. mains voltage prior to application of the test level. 3 A/m @ 50 Hz and 60 Hz Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment. Guidanc electromagnetic immunity The SmartPill GI Monitoring System is intended for use in the electromagnetic environment specified below. The user of the SmartPill GI Monitoring System should assure that it is used in such an environment. Immunity test Electromagnetic environment guidance Compliance level IEC 60601 test level 3 V 3 V/m 3 Vrms 150 kHz to 80 MHz 3 V/m 80 MHz to 2.5 GHz Conducted RF IEC 61000-

4-6 Radiated RF IEC 61000-

4-3 Portable and mobile RF communications equipment should be used no closer to any part of the SmartPill GI Monitoring System, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance d = 1.17 P d = 1.17 P 80 MHz to 800 MHz d = 2.33 P 800 MHz to 2.5 GHz where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey.

(a) should be less than the compliance level in each frequency range.

(b) Interference may occur in the vicinity of equipment marked with the following symbol:

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the SmartPill GI Monitoring System is used exceeds the applicable RF compliance level above, the SmartPill GI Monitoring System should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the SmartPill GI Monitoring System. b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m. Recommended separation distances between portable and mobile RF communications equipment and the SmartPill GI Monitoring System The SmartPill GI Monitoring System is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the SmartPill GI Monitoring System can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the SmartPill GI Monitoring System as recommended below, according to the maximum output power of the communications equipment. Rated maximum output power of transmitter W Separation distance according to frequency of transmitter m 150 kHz to 80 MHz d = 1.17 P 80 MHz to 800 MHz d = 1.17 P 800 MHz to 2,5 GHz d = 2.33 P 0.12 0.37 1.17 3.69 11.67 0.23 0.74 2.33 7.38 23.33 0.12 0.37 1.17 3.69 11.67 0,01 0,1 1 10 100 For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. Device Classifications SmartPill pH.p Capsule Power:

Electric Shock Protection:

Harmful Ingress Water:

Internally Powered Equipment Type BF Applied Part Watertight Equipment

(IP57) Equipment not suitable for use in the presence of FLAMMABLE ANAESTHETIC MIXTURE WITH AIR or WITH OXYGEN OR NITROUS OXIDE. Not for use with oxygen or oxygen enriched atmospheres. Intermittent operation SmartPill Data Receiver SmartPill Docking Station Internally Powered Equipment Class I Equipment Type BF Applied Part Ordinary Equipment Ordinary Equipment Ordinary Equipment Equipment not suitable for use in the presence of FLAMMABLE ANAESTHETIC MIXTURE WITH AIR or WITH OXYGEN OR NITROUS OXIDE. Not for use with oxygen or oxygen enriched atmospheres. Equipment not suitable for use in the presence of FLAMMABLE ANAESTHETIC MIXTURE WITH AIR or WITH OXYGEN OR NITROUS OXIDE. Not for use with oxygen or oxygen enriched atmospheres. Continuous Operation Continuous Operation Mode of Operation:

Connectivity Restrictions External equipment intended for connection to signal input, signal output or other connectors shall comply with IEC 60601 series for medical electrical equipment. In addition, all such combinations systems shall comply with the standard IEC 60601-

1-1, Safety requirements for medical electrical systems. Equipment not complying with IEC 60601-1 shall be kept outside the patient environment, as defined in the standard.5 Any person who connects external equipment to signal input, signal output or other connectors has formed a system and is responsible for the system to comply with the requirements of IEC 60601-1-1. If in doubt, contact a qualified biomedical professional or the SmartPill Corporation. Index 5 The normal distance is at least 1.5 m from the patient or the patient support. Accessories, 6 Activation Fixture, 5 Adverse Events, 13 Body Exit, 63, 82 Capsule Activation, 32 Confirming Exit, 45 Deactivating, 41 Low Voltage, 62 Operational Specifications, 2 Pack, 2 Power Requirements, 11 Tray Orientation, 36 Capsule Ingestion, 50 Chronic constipation, 9 Colonic transit time, 9 Combined small and large bowel transit time, 9 Contraindications, 10 CTT. See Colonic transit time Data Display. See Data Receiver Display Data Receiver, 3 Backlight Control Button, 3 Belt Clip and Lanyard, 3 Care, Cleaning and Maintenance, 14 Charging, 21 Display, 12 Event Button, 3 Patient Diary, 3 Power Requirements, 11 Device Markings, 11 Docking Station, 4 Care, Cleaning and Maintenance, 15 Connecting to the System Computer, 18 LED Light, 4 Power Connection, 4 Power Requirements, 10 USB Connector, 4 Exporting Data, 106 Gastric Emptying, 55, 81 Gastric emptying time, 9 Gastroparesis, 9 GET. See Gastric emptying time Graph Display, 96 ICJ. See Ileo-Cecal Junction Ileo-Cecal Junction, 60, Ingestion, 80 Installing Software, 112 Intended Use/Indications for Use, 9 Letterhead Creating, 93 Live Monitoring, 40 Medications, 22 MotiliGI Exiting, 90 Installing, 114 Keyboard Shortcuts, 88 Security, 110 Set up, 17 Uninstalling, 114 User Interface, 85 MotiliGI Administrator, 112 MotiliGI Software, 5 Non-Passage, 13 Patient Files Backing Up, 111 Patient Information Editing, 95 Patient Preparation, 22 Patient-Contacting Materials, 14 Power Requirements, 10 Recycling and Disposal Instructions, 11 Report Generating, 105 Risks and Safety, 13 SBTT. See Small bowel transit time SLBTT. See Combined small and large bowel transit time Small bowel transit time, 9 SmartBar, 2, 23 Statistics Calculating, 103 Storage, 10 System Computer, 5 Date, Time, Language and Regional Options, 17 Logging in, 109 Power Requirements, 10 Requirements, 6 Set up, 17 Templates Creating, 30 Using, 30 Test Analyzing, 49 Downloading, 43 Test Analysis Wizard, 47 Test Initiation Wizard, 27 Test Summary Reports, 76 Troubleshooting and Support, 15 User Preferences, 90 WGTT. See Whole gut transit time Whole gut transit time, 9 Windows Administrative Logon, 109 Contacting Given Imaging USA & Headquarters of the Americas Given Imaging, Inc. 3950 Shackleford Road, Suite 500 Duluth, GA 30096, USA Phone: 770-662-00870 Toll-Free: 1-800-GIVENGI Fax: 770-662-0510 USA: supportUS@givenimaging.com Latin America: supportLA@givenimaging.com Germany & European Headquarters Authorized Representative in the EU Given Imaging GmbH Borsteler Chaussee 47 Hamburg 22453 Germany Phone: +49 40 513 3000 Fax: +49 40 4606 9611 supportEU@givenimaging.com Canada Given Imaging, Inc. - Canadian Office 2425 Matheson Blvd. E., 8th Floor Mississauga, ON L4W 5K4 Canada Phone: 905 361 2830 Toll-Free: 1866 98 GIVEN Fax: 1 800 786 1967 supportCA@givenimaging.com France Given Imaging France S.A.S. 22, Rue Guynemer 78600 Maison-Laffitte Paris, France Phone: +33 (0) 1 34 93 80 00 Fax: +33 (0) 1 34 93 80 11 supportFR@givenimaging.com Australia & New Zealand Given Imaging Pty Limited Unit 6A, The Park 5 Talavera Road North Ryde, NSW 2113, Australia Phone: +61 2 9889 3944 Fax: +61 2 9889 3955 supportAU@givenimaging.com Asia Given Imaging (Asia) Company Limited 27/F. Unit A, Cheuk Nang Plaza 250 Hennessy Road, Wanchai Hong Kong Phone: +852 2989 0888 Fax: +852 2989 0899 supportAP@givenimaging.com Japan Given Imaging K.K. 2F KDX Kojimachi Bldg. 3-3 Kojimachi, Chiyoda-k Tokyo 102-0083 Japan Phone: + 81-3-5214-0588 supportJP@givenimaging.com This manual and the compilation of the content in this manual, including but not limited to text, graphics, logos and images, is the exclusive property of Given Imaging and is protected by United States and international copyright laws. This manual may not be transferred in any form without permission of Given Imaging. Copyright 2006-2013 Given Imaging. All Rights Reserved. The SmartPill logo, The Measure of GI Health and MotiliGI, are trademarks of Given Imaging. Such marks are protected by United States common law, federal and/or international trademark laws and may not be used in violation of Given Imagings rights. Given Imaging 3950 Shackleford Road Duluth, GA 30096 USA www.givenimaging.com