Skip to content

Cxi G23162

by Cook Incorporated

Ref CXI-2.3-14-135-ANG

Cxi G23162 (CXI-2.3-14-135-ANG) is a device classified as Class IIa in the EU and Class II in the US made by Cook Incorporated, registered in EUDAMED on 14 Sep 2026 (Basic UDI-DI B-00827002231627) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00827002231627), 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-00827002231627 Basic UDI-DI 00827002231627UDI-DIDate14 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00827002231627 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00827002231627 registered 14 Sep 2026 Active
  • FDA GUDID UDI-DI 00827002231627 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00827002231627
  2. Registered EUDAMED B-00827002231627

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  • Withdrawn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
Cxi® EUDAMED
Cxi GUDID
Generic name
Angiographic catheter, single-use
Model / Ref / Catalog
CXI-2.3-14-135-ANG, G23162
Primary DI / UDI-DI
00827002231627
Basic UDI-DI
B-00827002231627
FDA product code
KRA
EMDN code
C0104020101 Panoramic and selective peripheral diagnostic angiography catheters and microcatheters
GMDN term
Angiographic catheter, single-use
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
870.1210
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
CXI-2.3-14-135-ANG
GUDID
G23162
Device classEUDAMED
Class IIa
GUDID
Class II

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.

Related devices

Category: Angiographic catheter, single-use

Similar devices in this category

Other devices filed under PANORAMIC AND SELECTIVE PERIPHERAL DIAGNOSTIC ANGIOGRAPHY CATHETERS AND MICROCATHETERS.

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)