MotionWatch R
by CamNtech Ltd
Ref 04-125
MotionWatch R (04-125) is a Class I device made by CamNtech Ltd, registered in EUDAMED on 25 Jan 2023 (Basic UDI-DI ++B329MTN012J), active as of 22 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number++B329MTN012J B329MWR50L | Date25 Jan 2023 | StatusActive |
Official records
- EUDAMED public site ++B329MTN012J
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- MotionWatch
- Model / reference
- 04-125
- Primary DI / UDI-DI
- B329MWR50L
- Basic UDI-DI
- ++B329MTN012J
- Direct marketing DI
- B329MWR50L
- EMDN code
- Z12040199 General medicine diagnosis and monitoring instruments - other
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- GB-MF-000004683
- Authorised representative
- QbD RepS BV BE-AR-000000040
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