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Pocguide Multi-Drug Test Cup 1

by Hangzhou Aichek Medical Technology Co., Ltd. 4 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06978151200041 UDI-DI Date24 Dec 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Pocguide Multi-Drug Test Cup
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Model / Reference
1
Primary DI / UDI-DI
06978151200041
FDA Product Code
NFT, NGL, PTH, NFV, NFY, PTG, NGG, NGM, QAW, NFW
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Device Class
Class II
Regulation Number
862.3100, 862.3650, 862.3150, 862.3170, 862.3250, 862.3620, 862.3610, 862.3910, 862.3870
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multiple drugs of abuse IVD, kit, rapid ICT, clinical

Other devices from Hangzhou Aichek Medical Technology Co., Ltd.

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Properties

  • Single Use
  • Over-the-Counter
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No