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Pelvis plaster cast device 10033600

by Maquet, Inc.

Ref 10033600

Pelvis plaster cast device 10033600 is a Class I device made by Maquet, Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 40467680107EBM) and listed in FDA GUDID since 22 Sep 2022 (UDI-DI 04046768000230), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number40467680107EBM Basic UDI-DI 04046768000230UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04046768000230 UDI-DI Date22 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40467680107EBM registered 29 Oct 2026 Active
  • FDA GUDID UDI-DI 04046768000230 listed 22 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046768000230
  2. Registered EUDAMED 40467680107EBM

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Pelvis plaster cast device
Generic name
Operating table orthopaedic extension, non-powered
Device name
Traction pelvis plaster cast
Model / reference
10033600
Primary DI / UDI-DI
04046768000230
Basic UDI-DI
40467680107EBM
FDA product code
BWN
EMDN code
Z12011280 Patient positioning instruments - hardware accessories
GMDN term
Operating table orthopaedic extension, non-powered
Device class
Class I
Regulation number
878.4950
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Related devices

Category: Operating table orthopaedic extension, non-powered

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Maquet, Inc.

See all devices from Maquet, Inc. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)