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Cook G14230

by Cook Incorporated

Ref 050042

Cook G14230 (050042) is a fluid transfer tube (EU MDD Class I; FDA Class II; FDA product code FCN, Urinary drainage collection kit, for indwelling catheter) made by Cook Incorporated, registered in EUDAMED on 16 Jun 2026 (Basic UDI-DI B-00827002142305) and listed in FDA GUDID since 22 Aug 2017 (UDI-DI 00827002142305), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

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/MDD EUDAMED NumberB-00827002142305 Basic UDI-DI 00827002142305UDI-DIDate16 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00827002142305 UDI-DI Date22 Aug 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00827002142305 registered 16 Jun 2026 Active
  • FDA GUDID UDI-DI 00827002142305 listed 22 Aug 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00827002142305
  2. Registered EUDAMED B-00827002142305

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Cook
Generic name
Fluid transfer tube, general-purpose
Model / Ref / Catalog
050042, G14230
Primary DI / UDI-DI
00827002142305
Basic UDI-DI
B-00827002142305
FDA product code
FCN
EMDN code
A070199 Adapters and connectors - other
GMDN term
Fluid transfer tube, general-purpose
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.5250
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
050042
GUDID
G14230
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.

Similar devices in this category

Other devices filed under ADAPTERS AND CONNECTORS - OTHER.

Other devices from Cook Incorporated

See all devices from Cook Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (16, all answered No)