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7000 Series Leg Section

by Steris Corporation 5 variants

Ref BF00237Model Leg Positioner

7000 Series Leg Section (BF00237) is a Class I device made by Steris Corporation, registered in EUDAMED on 25 Sep 2026 (Basic UDI-DI 0724995MG7000LEGPSTNRGQ) and listed in FDA GUDID since 18 Oct 2024 (UDI-DI 00724995229283), 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 Number0724995MG7000LEGPSTNRGQ Basic UDI-DI 00724995229283UDI-DIDate25 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995229283 UDI-DI Date18 Oct 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995MG7000LEGPSTNRGQ registered 25 Sep 2026 Active
  • FDA GUDID UDI-DI 00724995229283 listed 18 Oct 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00724995229283
  2. Registered EUDAMED 0724995MG7000LEGPSTNRGQ

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  • Withdrawn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
Leg procedure positioner
Model / Ref / Catalog
Leg Positioner, BF00237, 7000 Series Leg Section
Primary DI / UDI-DI
00724995229283
Basic UDI-DI
0724995MG7000LEGPSTNRGQ
FDA product code
FQO
EMDN code
Z12011299 Patient positioning instruments – other
GMDN term
Leg procedure positioner
Device class
Class I
Regulation number
878.4960
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
Leg Positioner
BF00237
GUDID
7000 Series Leg Section

Related devices

Category: Leg procedure positioner

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)