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BF083

by Steris Corporation

Ref BF083Model Clamps and Locks

BF083 is a Class I device made by Steris Corporation, registered in EUDAMED on 1 Oct 2026 (Basic UDI-DI 0724995MGCLAMPLOCKSK) and listed in FDA GUDID since 23 Apr 2021 (UDI-DI 10724995191150), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0724995MGCLAMPLOCKSK Basic UDI-DI 10724995191150UDI-DIDate1 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10724995191150 UDI-DI Date23 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995MGCLAMPLOCKSK registered 1 Oct 2026 Active
  • FDA GUDID UDI-DI 10724995191150 listed 23 Apr 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10724995191150
  2. Registered EUDAMED 0724995MGCLAMPLOCKSK

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  • Withdrawn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
Medical table clamp
Device name
Clamps and Locks
Model / Ref / Catalog
BF083, Clamps and Locks
Primary DI / UDI-DI
10724995191150
Basic UDI-DI
0724995MGCLAMPLOCKSK
Unit of use DI
00724995191153
FDA product code
FWZ
EMDN code
Z12011280 Patient positioning instruments - hardware accessories
GMDN term
Medical table clamp
Device class
Class I
Regulation number
878.4950
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS - HARDWARE ACCESSORIES.

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)