FDA Device Intelligence
HomeHangzhou AllTest Biotech Co., Ltd. › DrugTect Multi-Drug Rapid Test Cup

DrugTect Multi-Drug Rapid Test Cup

Hangzhou AllTest Biotech Co., Ltd. · Model DT-AT12-1-AZ200 · UDI-DI 16942598201784

NFTPTHNGLNFVNFYNGGNGIPTGNFW
10
510(k) clearances
8
Adverse events
0
Recalls
50
Facilities

Description

DrugTect ,12 Panel Multi-Drug Test Cup, CLIA WAIVED (AMP500, BAR300, BUP10, BZO300,COC150, FYL1, MDMA500, MET500,MOP300, MTD300, OXY100, THC50) Contents: Test Cups - 200, Package Insert - 1, Security seals - 200. For In Vitro Diagnostic Use Only.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.