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Transfer board 113065A0

by Maquet, Inc.

Ref 113065A0

Transfer board 113065A0 is a Class I device made by Maquet, Inc., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 40467680102EB6) and listed in FDA GUDID since 22 Sep 2022 (UDI-DI 04046768002678), 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 Number40467680102EB6 Basic UDI-DI 04046768002678UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04046768002678 UDI-DI Date22 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40467680102EB6 registered 29 Oct 2026 Active
  • FDA GUDID UDI-DI 04046768002678 listed 22 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046768002678
  2. Registered EUDAMED 40467680102EB6

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  • Withdrawn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
Leg procedure positioner
Device name
Leg plate transfer board
Model / reference
113065A0
Primary DI / UDI-DI
04046768002678
Basic UDI-DI
40467680102EB6
FDA product code
BWN
EMDN code
Z12011280 Patient positioning instruments - hardware accessories
GMDN term
Leg procedure positioner
Device class
Class I
Regulation number
878.4950
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Maquet, Inc.

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Properties

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