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Cook G03301

by Cook Incorporated

Ref C-TPT-100

Cook G03301 (C-TPT-100) is a device classified as Class IIa in the EU and Class II in the US made by Cook Incorporated, registered in EUDAMED on 20 Jul 2026 (Basic UDI-DI B-00827002033016) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00827002033016), 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-00827002033016 Basic UDI-DI 00827002033016UDI-DIDate20 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00827002033016 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00827002033016 registered 20 Jul 2026 Active
  • FDA GUDID UDI-DI 00827002033016 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00827002033016
  2. Registered EUDAMED B-00827002033016

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  • Withdrawn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
Pleural/peritoneal drainage catheterization kit, non-medicated
Model / Ref / Catalog
C-TPT-100, G03301
Primary DI / UDI-DI
00827002033016
Basic UDI-DI
B-00827002033016
FDA product code
JOL
EMDN code
A060203 Pleural drainages with valve and kits
GMDN term
Pleural/peritoneal drainage catheterization kit, non-medicated
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
880.6740
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
C-TPT-100
GUDID
G03301
Device classEUDAMED
Class IIa
GUDID
Class II
ImplantableEUDAMED
No
GUDID
Yes

Device class is stated on each registry's own scale: Class IIa 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 PERCUTANEOUS DRAINAGE SYSTEMS.

Other devices from Cook Incorporated

See all devices from Cook Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Implantable NoEUDAMEDYesGUDID
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (15, all answered No)