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Universal Remote Control 1009251

by Maquet, Inc.

Ref 100925B1

Universal Remote Control 1009251 (100925B1) is a Class I device made by Maquet, Inc., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI 40467680112AB3) and listed in FDA GUDID since 20 Mar 2024 (UDI-DI 04046768150966), 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 Number40467680112AB3 Basic UDI-DI 04046768150966UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04046768150966 UDI-DI Date20 Mar 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40467680112AB3 registered 30 Oct 2026 Active
  • FDA GUDID UDI-DI 04046768150966 listed 20 Mar 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046768150966
  2. Registered EUDAMED 40467680112AB3

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  • Withdrawn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
Universal Remote Control
Generic name
Operating room equipment remote control
Device name
Hand control
Model / Ref / Catalog
100925B1, 1009251
Primary DI / UDI-DI
04046768150966
Basic UDI-DI
40467680112AB3
FDA product code
FQO
EMDN code
Z12011202 Operating tables
GMDN term
Operating room equipment remote control
Device class
Class I
Regulation number
878.4960
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
Model / referenceEUDAMED
100925B1
GUDID
1009251

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Properties

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