Accu-Chek® Insight CGM app (Unreleased)

The Accu-Chek Insight CGM app is used to operate and set up the Accu-Chek Insight CGM system. The Accu-Chek Insight CGM system is a system for continuous glucose monitoring, which means it continuously measures the glucose concentration in the interstitial fluid and delivers results continuously. The CGM app receives and saves the continuous glucose monitoring results. The user can enter additional information in the CGM app. This could be blood glucose results, carbohydrate amounts consumed, insulin amounts and health events (for example, exercise or illness). The CGM app displays the continuous glucose monitoring results and the entered information on the smartphone screen. The CGM app may only be used together with the other components of the Accu-Chek Insight CGM system (sensor and transmitter). The complete User’s Manual for the Accu-Chek Insight CGM system is contained in the packaging of the Accu-Chek Insight CGM transmitter.
The Accu-Chek Insight CGM app only runs on smartphones which meet the following specifications:
• HTC One M7®
• Screen: 4.7 inch, full HD 1080p, 468 PPI, resolution: 720 x 1280: xhdpi
• Android version: 4.4.2.
If you need help using this app, contact your customer support; contact information can be found at www.accu-chek.com.
Information on the Bluetooth® connection:
The CGM app uses a Bluetooth connection (Bluetooth Low Energy = BLE) to receive the data from the CGM transmitter.
Information on the required permissions:
The CGM app does not require any permissions.
Version 10.00
ACCU-CHEK and ACCU-CHEK INSIGHT are trademarks of Roche.
The Bluetooth ® word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any use of such marks by Roche is under license.
ANDROID and GOOGLE PLAY are trademarks of Google Inc.
All other product names and trademarks are the property of their respective owners.
© 2016 Roche Diabetes Care
Manufacturer:
Roche Diabetes Care GmbH
Sandhofer Strasse 116
68305 Mannheim, Germany
www.accu-chek.com

CE 0088

This product fulfils the requirements of the European Directive 93/42/EEC on medical devices.