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The Web G22303

by Cook Incorporated

Ref MSB-35-2X4

The Web G22303 (MSB-35-2X4) is a device classified as Class I in the EU and Class II in the US made by Cook Incorporated, registered in EUDAMED on 7 May 2026 (Basic UDI-DI B-00827002223035) and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00827002223035), 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-00827002223035 Basic UDI-DI 00827002223035UDI-DIDate7 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00827002223035 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00827002223035 registered 7 May 2026 Active
  • FDA GUDID UDI-DI 00827002223035 listed 24 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00827002223035
  2. Registered EUDAMED B-00827002223035

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  • Withdrawn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
The Web
Generic name
Biliary/urinary stone retrieval basket, single-use
Model / Ref / Catalog
MSB-35-2X4, G22303
Primary DI / UDI-DI
00827002223035
Basic UDI-DI
B-00827002223035
FDA product code
LQR
EMDN code
G0305010202 Digestive endoscopy, retrieval basket devices, non-revolving
GMDN term
Biliary/urinary stone retrieval basket, single-use
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.5010
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
MSB-35-2X4
GUDID
G22303
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 DIGESTIVE ENDOSCOPY, RETRIEVAL BASKET DEVICES, NON-REVOLVING.

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)