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Kenevo A-B-C

Qualified therapy personnel can use the Kenevo A-B-C to adjust the settings of Kenevo prostheses

Qualified therapy personnel can use the Kenevo A-B-C to adjust the settings of Kenevo prostheses

Kenevo A-B-C

by Ottobock SE & Co. KGaA
Kenevo A-B-C
Kenevo A-B-C
Kenevo A-B-C

What is it about?

Qualified therapy personnel can use the Kenevo A-B-C to adjust the settings of Kenevo prostheses. This allows the prosthesis settings to be optimised for the patient’s current level of mobility. Key functions are:

Kenevo A-B-C

App Details

Version
1.2
Rating
NA
Size
95Mb
Genre
Medical Utilities
Last updated
January 26, 2024
Release date
December 18, 2019
More info

App Screenshots

Kenevo A-B-C screenshot-0
Kenevo A-B-C screenshot-1
Kenevo A-B-C screenshot-2
Kenevo A-B-C screenshot-3
Kenevo A-B-C screenshot-4

App Store Description

Qualified therapy personnel can use the Kenevo A-B-C to adjust the settings of Kenevo prostheses. This allows the prosthesis settings to be optimised for the patient’s current level of mobility. Key functions are:
- Switching between activity modes A, B, B+ and C
- Adapting stance phase flexion resistance
- Configuring wheelchair functions
- Configuring intuitive stance
With Kenevo A-B-C, you can also set up and manage your MyOttobock account.

Requirements for using the app are proof of professional qualifications, Kenevo therapist training and passing the online certification test.
The instructions for use are available in this app in electronic form as a PDF file. A third-party app is required to open PDF files.
We are required to remind you to seek a doctor’s advice in addition to using this app and before making any medical decisions.

Only Kenevo prostheses sold in or after January 2019 are also compatible with Apple mobile devices.
Please contact your local Ottobock branch or myottobock@ottobock.com for further information.

Manufacturer:
Otto Bock Healthcare Products GmbH
Brehmstrasse 16 · 1110 Vienna · Austria
T +43 1 523 37 86 · F +43 1 523 22 64
www.ottobock.com

This product meets the applicable European requirements for medical devices.

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