Therafit Belts 62203
Ref 62203
Therafit Belts 62203 is a Class I device made by Therafin Corporation, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 0840252962203U9) and listed in FDA GUDID since 6 Jul 2023 (UDI-DI 00840252902086), active as of 7 Nov 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 | Number0840252962203U9 00840252902086 | Date4 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00840252902086 | Date6 Jul 2023 | StatusListed |
Official records
- EUDAMED public site 0840252962203U9
- AccessGUDID record 00840252902086
Across registries
- EUDAMED Basic UDI-DI 0840252962203U9 registered 4 Nov 2026 Active
- FDA GUDID UDI-DI 00840252902086 listed 6 Jul 2023 Listed
Timeline
- Listed FDA GUDID 00840252902086
- Registered EUDAMED 0840252962203U9
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Hip Belt, 1.5" TheraFit Single Pull, PB Buckle, 9.25 x 2.5 Pads w/ Clips, Cams EUDAMEDTherafit Belts GUDID
- Generic name
- Wheelchair/chair/stander occupant restraint/support
- Model / Ref / Catalog
- 62203
- Primary DI / UDI-DI
- 00840252902086
- Basic UDI-DI
- 0840252962203U9
- FDA product code
- ISR
- EMDN code
- Y122406 Belts, seats and armrests for wheelchairs
- GMDN term
- Wheelchair/chair/stander occupant restraint/support
- Device class
- Class I
- Regulation number
- 890.3025
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
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