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Side rail clamp 100725F0

by Maquet, Inc.

Ref 100725F0

Side rail clamp 100725F0 is a spinal surgery positioning board (EU MDR Class I; FDA Class I; FDA product code BWN, Table and Attachments, Operating-Room) made by Maquet, Inc., registered in EUDAMED on 30 Oct 2026 (Basic UDI-DI 40467680132DBK) and listed in FDA GUDID since 22 Sep 2022 (UDI-DI 04046768114258), 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 Number40467680132DBK Basic UDI-DI 04046768114258UDI-DIDate30 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04046768114258 UDI-DI Date22 Sep 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40467680132DBK registered 30 Oct 2026 Active
  • FDA GUDID UDI-DI 04046768114258 listed 22 Sep 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046768114258
  2. Registered EUDAMED 40467680132DBK

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  • Withdrawn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
Side rail clamp
Generic name
Spinal surgery positioning board
Device name
Universal frame clamp
Model / reference
100725F0
Primary DI / UDI-DI
04046768114258
Basic UDI-DI
40467680132DBK
FDA product code
BWN
EMDN code
Z12011280 Patient positioning instruments - hardware accessories
GMDN term
Spinal surgery positioning board
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: Spinal surgery positioning 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)