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Transfer board 1180.71C0

by Maquet, Inc.

Ref 118071C0

Transfer board 1180.71C0 is a patient transfer sliding board (EU MDR Class I; FDA Class II; FDA product code IXQ, Table, Radiographic, Stationary Top) made by Maquet, Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 40467680128ABS) and listed in FDA GUDID since 6 Feb 2019 (UDI-DI 04046768132061), 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 Number40467680128ABS Basic UDI-DI 04046768132061UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04046768132061 UDI-DI Date6 Feb 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40467680128ABS registered 29 Oct 2026 Active
  • FDA GUDID UDI-DI 04046768132061 listed 6 Feb 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046768132061
  2. Registered EUDAMED 40467680128ABS

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  • Withdrawn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
Transfer board
Generic name
Patient transfer sliding board
Model / reference
118071C0 EUDAMED
1180.71C0 GUDID
Primary DI / UDI-DI
04046768132061
Basic UDI-DI
40467680128ABS
FDA product code
IXQ
EMDN code
Z12011280 Patient positioning instruments - hardware accessories
GMDN term
Patient transfer sliding board
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
MRI safety
MR Conditional

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
118071C0
GUDID
1180.71C0
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.

Related devices

Category: Patient transfer sliding board

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)