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FD256

by Corporation Steris Canada

Ref FD256Model RAS Cycle Rack

FD256 is a device classified as Class I in the EU and Class II in the US made by Corporation Steris Canada, registered in EUDAMED on 25 Jun 2026 (Basic UDI-DI 0724995QBRASCYCLERACK9J) and listed in FDA GUDID since 9 Sep 2019 (UDI-DI 00724995176723), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0724995QBRASCYCLERACK9J Basic UDI-DI 00724995176723UDI-DIDate25 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995176723 UDI-DI Date9 Sep 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995QBRASCYCLERACK9J registered 25 Jun 2026 Active
  • FDA GUDID UDI-DI 00724995176723 listed 9 Sep 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00724995176723
  2. Registered EUDAMED 0724995QBRASCYCLERACK9J

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  • Withdrawn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
Luminal device flushing tubing set, reusable
Device name
RAS Cycle Rack
Model / Ref / Catalog
FD256, RAS Cycle Rack
Primary DI / UDI-DI
00724995176723
Basic UDI-DI
0724995QBRASCYCLERACK9J
FDA product code
NVE
EMDN code
Z12011380 Cleaning, disinfection and sterilisation instruments - hardware accessories
GMDN term
Luminal device flushing tubing set, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.1500
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
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Luminal device flushing tubing set, reusable

Similar devices in this category

Other devices filed under CLEANING, DISINFECTION AND STERILISATION INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Corporation Steris Canada

See all devices from Corporation Steris Canada →

Properties

  • Over-the-counter
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)