Idm-Ms
by mo-vis bv
Ref PRSPS00010Model P014
Idm-Ms (PRSPS00010) is a timer switch (EU MDR Class I; FDA Class I; FDA product code KNN, Components, Wheelchair) made by mo-vis bv, registered in EUDAMED on 26 Mar 2025 (Basic UDI-DI 540700832MULTISWITCHHM) and listed in FDA GUDID since 3 Mar 2022 (UDI-DI 05407008320805), active as of 22 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number540700832MULTISWITCHHM 05407008320805 | Date26 Mar 2025 | StatusActive |
| United States | GUDID listing GUDID | Number05407008320805 | Date3 Mar 2022 | StatusListed |
Official records
- EUDAMED public site 540700832MULTISWITCHHM
- AccessGUDID record 05407008320805
Across registries
- EUDAMED Basic UDI-DI 540700832MULTISWITCHHM registered 26 Mar 2025 Active
- FDA GUDID UDI-DI 05407008320805 listed 3 Mar 2022 Listed
Timeline
- Listed FDA GUDID 05407008320805
- Registered EUDAMED 540700832MULTISWITCHHM
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Idm-Ms EUDAMEDmo-Vis GUDID
- Generic name
- Timer switch
- Device name
- Multi Switch
- Model / reference
- P014 EUDAMEDPRSPS00010 EUDAMEDIDM-MS GUDID
- Primary DI / UDI-DI
- 05407008320805
- Basic UDI-DI
- 540700832MULTISWITCHHM
- FDA product code
- KNN
- EMDN code
- Y122403 Wheelchair footrests, supports and controls
- GMDN term
- Timer switch
- Device class
- Class I
- Regulation number
- 890.3920
- System or procedure pack
- System which is a device in itself
- EU registration type
- Standard device
- EU market of registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | P014 PRSPS00010 | IDM-MS |
Manufacturer details
- EUDAMED SRN
- BE-MF-000000729
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