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Multimodality transfer table top 118012A0

by Maquet, Inc.

Ref 118012A0

Multimodality transfer table top 118012A0 is a device classified as Class I in the EU and Class II in the US made by Maquet, Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 40467680129BBX) and listed in FDA GUDID since 22 Sep 2022 (UDI-DI 04046768132948), 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 Number40467680129BBX Basic UDI-DI 04046768132948UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04046768132948 UDI-DI Date22 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40467680129BBX registered 29 Oct 2026 Active
  • FDA GUDID UDI-DI 04046768132948 listed 22 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046768132948
  2. Registered EUDAMED 40467680129BBX

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  • Withdrawn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
Multimodality transfer table top
Generic name
Universal operating table top
Device name
Transfer table top multimodality
Model / reference
118012A0
Primary DI / UDI-DI
04046768132948
Basic UDI-DI
40467680129BBX
FDA product code
IXQ
EMDN code
Z12011280 Patient positioning instruments - hardware accessories
GMDN term
Universal operating table top
Device class
Class I EUDAMED
Class II GUDID
Regulation number
892.1980
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

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Properties

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