iBed Wireless 521200380100
Ref 521200380100Model 08858251002473SZ
iBed Wireless 521200380100 is a hospital stretcher (EU MDR Class I; FDA Class II; FDA product code FNL, Bed, Ac-Powered Adjustable Hospital) made by Stryker Corp., registered in EUDAMED on 16 Jun 2026 (Basic UDI-DI 08858251002473SZ) and listed in FDA GUDID since 20 Aug 2020 (UDI-DI 07613327520453), active as of 23 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 | Number08858251002473SZ 07613327520453 | Date16 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07613327520453 | Date20 Aug 2020 | StatusListed |
Official records
- EUDAMED public site 08858251002473SZ
- AccessGUDID record 07613327520453
Across registries
- EUDAMED Basic UDI-DI 08858251002473SZ registered 16 Jun 2026 Active
- FDA GUDID UDI-DI 07613327520453 listed 20 Aug 2020 Listed
Timeline
- Listed FDA GUDID 07613327520453
- Registered EUDAMED 08858251002473SZ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- iBed Wireless
- Generic name
- Hospital stretcher, powered
- Model / Ref / Catalog
- 521200380100, 08858251002473SZ
- Primary DI / UDI-DI
- 07613327520453
- Basic UDI-DI
- 08858251002473SZ
- Direct marketing DI
- 07613327520453
- FDA product code
- FNL
- EMDN code
- V08068099 Medical beds - other accessories
- GMDN term
- Hospital stretcher, powered
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 880.5100
- EU registration type
- Standard device
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class I | Class II |
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