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PowerLift Plus

by Steris Corporation

Ref BF867Model Power Lift Stirrups

PowerLift Plus (BF867) is a Class I device made by Steris Corporation, registered in EUDAMED on 20 Oct 2026 (Basic UDI-DI 0724995MGPOWLFTSTIRUP8F) and listed in FDA GUDID since 20 Dec 2022 (UDI-DI 00724995217280), 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 Number0724995MGPOWLFTSTIRUP8F Basic UDI-DI 00724995217280UDI-DIDate20 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995217280 UDI-DI Date20 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995MGPOWLFTSTIRUP8F registered 20 Oct 2026 Active
  • FDA GUDID UDI-DI 00724995217280 listed 20 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00724995217280
  2. Registered EUDAMED 0724995MGPOWLFTSTIRUP8F

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  • Withdrawn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
Heel stirrup
Device name
Power Lift Stirrups
Model / Ref / Catalog
Power Lift Stirrups, BF867, PowerLift Plus
Primary DI / UDI-DI
00724995217280
Basic UDI-DI
0724995MGPOWLFTSTIRUP8F
FDA product code
EYD
EMDN code
Z12011299 Patient positioning instruments – other
GMDN term
Heel stirrup
Device class
Class I
Regulation number
876.4890
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
Power Lift Stirrups
BF867
GUDID
PowerLift Plus

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

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