Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0
Let the assistant research this device
The Research Assistant compiles risk class, certificates, notified bodies and related records — and cites every one.
Free to try · every answer cites its records
Basic Information
- Primary DI
- 9120112972000
- Basic UDI-DI Code
- 9120112972006E
- Reference
- 200
- Device Types
- None provided
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 1
- Status
- On The Market
- Manufacturer
- Aurimod GmbH
Additional Description
The VIVO Pen is intended for use only in combination with VIVO in professional and home healthcare environments by qualified medical personnel and briefed patients to allow the adaptation of the stimulation intensity of VIVO in a predefined range for a patient specific therapy by using a magnetic field.
CND Nomenclature Codes
| Code | Description |
|---|---|
| V0880 | MEDICAL SUPPORT EQUIPMENT - ACCESSORIES |
Similar Devices
Other on-the-market devices with the same classification (Eu Md Class 1) and regulation (EU MDR).
ORTHODONTIC DEVICES - OTHER
Device
EU MDR
·
Eu Md Class 1
·LEONE S.P.A.·On the market·32 countries
Catalyst 5
Device
EU MDR
·
Eu Md Class 1
·Ki Mobility LLC·On the market
Catalyst 4
Device
EU MDR
·
Eu Md Class 1
·Ki Mobility LLC·On the market
Catalyst 5VX
Device
EU MDR
·
Eu Md Class 1
·Ki Mobility LLC·On the market
Little Wave Spark
Device
EU MDR
·
Eu Md Class 1
·Ki Mobility LLC·On the market
Little Wave Clik
Device
EU MDR
·
Eu Md Class 1
·Ki Mobility LLC·On the market