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U-Catch U-Catch Cotinine (COT) Test Dip Card

by Shenzhen Bioeasy Biotechnology Co., Ltd. 2 variants

U-Catch U-Catch Cotinine (COT) Test Dip Card (YRLG27801010) is a Class I device made by Shenzhen Bioeasy Biotechnology Co., Ltd., listed in FDA GUDID since 8 Dec 2022 (UDI-DI 06972428161349), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06972428161349 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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
U-Catch
Generic name
Cotinine IVD, kit, rapid ICT, clinical
Model / Ref / Catalog
U-Catch Cotinine (COT) Test Dip Card, YRLG27801010
Primary DI / UDI-DI
06972428161349
FDA product code
MRS
GMDN term
Cotinine IVD, kit, rapid ICT, clinical
Device class
Class I
Regulation number
862.3220
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cotinine IVD, kit, rapid ICT, clinical

Similar devices

Other devices filed under FDA product code MRS (Test System, Nicotine, Cotinine, Metabolites).

Other devices from Shenzhen Bioeasy Biotechnology Co., Ltd.

See all devices from Shenzhen Bioeasy Biotechnology Co., Ltd. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)