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Alltest Multi-Drug 13 Drugs Rapid Urine Test Panel DUA-A1134C-008

by Hangzhou AllTest Biotech Co., Ltd.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number16936983172414 UDI-DI Date14 Apr 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Alltest Multi-Drug 13 Drugs Rapid Urine Test Panel
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Model / Ref / Catalog
DUA-A1134C-008, DUA-A1134C
Description
25T, CLIA WAIVED, white package, AMP500/BAR300/BZO300/COC150/THC50/MTD300/MET500/MDMA500/MOP300/PCP25/TCA1000/OXY100/FYL1+OXI/SG/PH
Primary DI / UDI-DI
16936983172414
510(k) Number
FDA Product Code
NGL, NFT, NFY, NGG, NFW, CEN, NGM, QAW, PTG, NFV, PTH
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Device Class
Class II
Regulation Number
862.3650, 862.3100, 862.3250, 862.3610, 862.3870, 862.1550, 862.3910, 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