VitaliTENS
actiTENS kit : The actiTENS is a connected medical device for transcutaneous electrical neurostimulation intended to treat pain in adults and intended for persons over 18 years of age with unimpaired intellectual abilities coffret VitaliTENS : VitaliTENS is a medical device for transcutaneous electrical neurostimulation intended to treat chronic pain in adults suffering from knee osteoarthritis
Basic Information
- Primary DI
- 03770018808062
- Basic UDI-DI Code
- 3770018808SBMKitCoffretZH
- Reference
- 8703648
- Device Types
- None provided
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 2a
- Status
- On The Market
Additional Description
VitaliTENS is a medical device for transcutaneous electrical neurostimulation intended to treat chronic pain in adults suffering from knee osteoarthritis. VitaliTENS is fixed directly on to the body using a dedicated accessory. It adapts to the shape of your body with its flexible design. VitaliTENS can be used discreetly during your daily activities. It is operated through a smartphone app that allows you to choose from several stimulation programs and to save all the information recorded from the stimulation treatment sessions. VitaliTENS shares the same development as the actiTENS product, it is intended to relieve chronic pain in the context of gonarthrosis. It is therefore a reduction in the scope of application of actiTENS.
Medical Purpose
actiTENS kit : The actiTENS is a connected medical device for transcutaneous electrical neurostimulation intended to treat pain in adults and intended for persons over 18 years of age with unimpaired intellectual abilities coffret VitaliTENS : VitaliTENS is a medical device for transcutaneous electrical neurostimulation intended to treat chronic pain in adults suffering from knee osteoarthritis
CND Nomenclature Codes
| Code | Description |
|---|---|
| Z120601 | ELECTROTHERAPY EQUIPMENT (INCLUDED TENS) [correction as of 2025-01-01] |
Related Devices
The Basic UDI-DI associated with this device has 3 devices in total. Below are some other devices sharing the same Basic UDI-DI.
Similar Devices
Other on-the-market devices with the same classification (Eu Md Class 2a) and regulation (EU MDR).