Pelvic extension H V UK
by Baxter Medical Systems GmbH + Co. KG
Ref 2072629
Pelvic extension H V UK (2072629) is a Class I device made by Baxter Medical Systems GmbH + Co. KG, registered in EUDAMED on 18 Mar 2026 (Basic UDI-DI 0887761GMN000008U4) and listed in FDA GUDID since 15 Dec 2022 (UDI-DI 00887761970144), active (EUDAMED), not in commercial distribution (GUDID) as of 24 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 | Number0887761GMN000008U4 00887761970144 | Date18 Mar 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00887761970144 | Date15 Dec 2022 | StatusListed |
Official records
- EUDAMED public site 0887761GMN000008U4
- AccessGUDID record 00887761970144
Across registries
- EUDAMED Basic UDI-DI 0887761GMN000008U4 registered 18 Mar 2026 Active
- FDA GUDID UDI-DI 00887761970144 listed 15 Dec 2022 Listed
Timeline
- Listed FDA GUDID 00887761970144
- Registered EUDAMED 0887761GMN000008U4
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Pelvic extension H V UK EUDAMEDPelvis Sections GUDID
- Generic name
- Operating table orthopaedic extension, non-powered
- Model / reference
- 2072629
- Primary DI / UDI-DI
- 00887761970144
- Basic UDI-DI
- 0887761GMN000008U4
- FDA product code
- JEA, GDC, KXJ
- EMDN code
- Z12011280 Patient positioning instruments - hardware accessories
- GMDN term
- Operating table orthopaedic extension, non-powered
- Device class
- Class I
- Regulation number
- 878.4960, 892.1980
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- Not in Commercial Distribution
Manufacturer details
- EUDAMED SRN
- DE-MF-000005071
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