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Cook G14121

by Cook Incorporated

Ref 050043

Cook G14121 (050043) is a fluid transfer tube (EU MDD Class I; FDA Class II; FDA product code KNS, Unit, electrosurgical, endoscopic (with or without accessories)) made by Cook Incorporated, registered in EUDAMED on 16 Jun 2026 (Basic UDI-DI B-00827002141216) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00827002141216), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00827002141216 Basic UDI-DI 00827002141216UDI-DIDate16 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00827002141216 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00827002141216 registered 16 Jun 2026 Active
  • FDA GUDID UDI-DI 00827002141216 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00827002141216
  2. Registered EUDAMED B-00827002141216

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  • Withdrawn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
050043, G14121
Primary DI / UDI-DI
00827002141216
Basic UDI-DI
B-00827002141216
FDA product code
KNS
EMDN code
A070199 Adapters and connectors - other
GMDN term
Fluid transfer tube, general-purpose
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.4300
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
050043
GUDID
G14121
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: Fluid transfer tube, general-purpose

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
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (17, all answered No)