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Sacral Rest

by Steris Corporation 2 variants

Part of a family of 10 devices: see the family page

Ref BF00073Model Sacral Rest

Sacral Rest (BF00073) is a Class I device made by Steris Corporation, registered in EUDAMED on 1 Oct 2026 (Basic UDI-DI 0724995MGSACRALRESTV4) and listed in FDA GUDID since 2 Apr 2021 (UDI-DI 00724995158071), 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 Number0724995MGSACRALRESTV4 Basic UDI-DI 00724995158071UDI-DIDate1 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995158071 UDI-DI Date2 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995MGSACRALRESTV4 registered 1 Oct 2026 Active
  • FDA GUDID UDI-DI 00724995158071 listed 2 Apr 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00724995158071
  2. Registered EUDAMED 0724995MGSACRALRESTV4

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  • Withdrawn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
Operating table orthopaedic extension, non-powered
Model / Ref / Catalog
Sacral Rest, BF00073
Primary DI / UDI-DI
00724995158071
Basic UDI-DI
0724995MGSACRALRESTV4
FDA product code
CCX
EMDN code
Z12011299 Patient positioning instruments – other
GMDN term
Operating table orthopaedic extension, non-powered
Device class
Class I
Regulation number
868.6820
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Related devices

Category: Operating table orthopaedic extension, non-powered

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)