Skip to content

Alltest Multi-Drug 14 Urine Test Panel

by Hangzhou AllTest Biotech Co., Ltd. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06942598200766 UDI-DIDate13 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  • Withdrawn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-A1144H
Description
EN, 1T, MOP300/MDMA500/OXY100/PCP25/MTD300/BAR300 /BZO300/AMP500/TCA1000/COC150/MET500/THC50/ BUP10/FYL1
Primary DI / UDI-DI
06942598200766
510(k) Number
FDA Product Code
NGL, NFY, NGG, NFW, NFV, NGM, PTH, QAW, NFT, PTG
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Device Class
Class II
Regulation Number
862.3650, 862.3250, 862.3610, 862.3870, 862.3170, 862.3150, 862.3910, 862.3100, 862.3620
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K242540)

Show all (12)

Other devices from Hangzhou Alltest Biotech.Co., Ltd.

See all devices from Hangzhou Alltest Biotech.Co., Ltd. →

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