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BF00252

by Steris Corporation

Ref BF00252Model Universal Table Top

BF00252 is a Class I device made by Steris Corporation, registered in EUDAMED on 25 Sep 2026 (Basic UDI-DI 0724995MG7000UNVTBTOPWK) and listed in FDA GUDID since 25 Nov 2024 (UDI-DI 00724995229337), active as of 24 Oct 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0724995MG7000UNVTBTOPWK Basic UDI-DI 00724995229337UDI-DIDate25 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995229337 UDI-DI Date25 Nov 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995MG7000UNVTBTOPWK registered 25 Sep 2026 Active
  • FDA GUDID UDI-DI 00724995229337 listed 25 Nov 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00724995229337
  2. Registered EUDAMED 0724995MG7000UNVTBTOPWK

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  • Withdrawn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

Generic name
Universal operating table top
Device name
Universal Table Top
Model / Ref / Catalog
BF00252, Universal Table Top
Primary DI / UDI-DI
00724995229337
Basic UDI-DI
0724995MG7000UNVTBTOPWK
FDA product code
FMR
EMDN code
Z12011299 Patient positioning instruments – other
GMDN term
Universal operating table top
Device class
Class I
Regulation number
880.6785
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Related devices

Category: Universal operating table top

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS – OTHER.

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Over-the-counter
  • Premarket exempt
  • Manufacturing date
Other properties (22, all answered No)