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Cook G01942

by Cook Incorporated

Cook G01942 (C-SF-35-50) is a Class II device made by Cook Incorporated, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00827002019423), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00827002019423 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Cook
Generic name
Peripheral vascular guidewire, manual
Model / Ref / Catalog
G01942, C-SF-35-50
Primary DI / UDI-DI
00827002019423
FDA product code
DQX
GMDN term
Peripheral vascular guidewire, manual
Device class
Class II
Regulation number
870.1330
GUDID distribution status
In Commercial Distribution

Related devices

Category: Peripheral vascular guidewire, manual

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 (9, all answered No)