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BF00245

by Steris Corporation

Ref BF00245Model Arm Positioner

BF00245 is a Class I device made by Steris Corporation, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI 0724995MG7000ARMPSTNRKJ) and listed in FDA GUDID since 25 Nov 2024 (UDI-DI 00724995224950), 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 Number0724995MG7000ARMPSTNRKJ Basic UDI-DI 00724995224950UDI-DIDate5 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995224950 UDI-DI Date25 Nov 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995MG7000ARMPSTNRKJ registered 5 Nov 2026 Active
  • FDA GUDID UDI-DI 00724995224950 listed 25 Nov 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00724995224950
  2. Registered EUDAMED 0724995MG7000ARMPSTNRKJ

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  • Withdrawn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
Arm procedure positioner, reusable
Device name
Arm Positioner
Model / Ref / Catalog
BF00245, Arm Positioner
Primary DI / UDI-DI
00724995224950
Basic UDI-DI
0724995MG7000ARMPSTNRKJ
FDA product code
GBB
EMDN code
Z12011299 Patient positioning instruments – other
GMDN term
Arm procedure positioner, reusable
Device class
Class I
Regulation number
878.4960
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Related devices

Category: Arm procedure positioner, reusable

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
  • Serial number
  • Manufacturing date
Other properties (21, all answered No)