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Alltest Multi-Drug 12 Drugs Urine Test Panel

by Hangzhou AllTest Biotech Co., Ltd. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number16936983170007 UDI-DIDate15 Apr 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Model / Ref / Catalog
1, DOA-A1124C
Description
25T, CLIA WAIVED, white package MOP300/MDMA500/OXY100/MTD300/BAR300/BZO300/AMP500/COC150/MET500/THC50/BUP10/FYL1
Primary DI / UDI-DI
16936983170007
510(k) Number
FDA Product Code
NFY, NFT, NGG, NGL, NFW, PTG, NFV, PTH
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Device Class
Class II
Regulation Number
862.3250, 862.3100, 862.3610, 862.3650, 862.3870, 862.3620, 862.3170, 862.3150
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K242540)

Show all (12)

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Properties

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

Other properties (10)

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