Technical Specifications Medications Supported Dimensions: 3.5 cm wide, 7 cm tall Battery life: 14 months expected, 6 months guaranteed CR 2032 battery Tactile Switch, 100,000 cycle min, 0.2 mm Bluetooth 4.0 LE Records date and time stamp of medication dose Medication use sent and received passively with no additional steps required by user Memory for 28 doses. Dose history remains in memory until data transmission sent and received by mobile app Splash resistant FCC, CE, Bluetooth certifications received
+ AEROBID
+ PROVENTIL HFA
+ ALBUTEROL
+ QVAR
+ ALUPENT HFA
+ SEREVENT
+ ALVESCO
+ SYMBICORT
+ ATROVENT HFA
+ VENTOLIN HFA
+ XOPENEX HFA
+ DULERA
+ FLOVENT
+ INTAL
+ PROAIR HFA Diskus and Non Standard Form Factor MDI HeroTrackers also available, on request C M Y CM MY CY CMY K NOTE: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:
Reorient or relocate the receiving antenna. Increase the separation between the equipment and receiver. Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. Consult the dealer or an experienced radio/TV technician for help. This device complies with part 15 of the FCC Rules. Operation is subject to the following two conditions:
(1) This device may not cause harmful interference, and
(2) this device must accept any interference received, including interference that may cause undesired operation. Changes or modifications not expressly approved by the party responsible for compliance could void the users authority to operate the equipment. coherohealth.com support@coherohealth.com @coherohealth facebook.com/coherohealth Cohero Health | CoheroHealth, LLC 2015