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DrugTect Multi-Drug Rapid Test Cup

Hangzhou AllTest Biotech Co., Ltd. · Model 1 · UDI-DI 06936983197526

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10
510(k) clearances
34
Adverse events
0
Recalls
52
Facilities

Description

2T, EN, (MOP300/MDMA500/OXY100/PCP25/COC150/MTD300/BAR300/BZO300/AMP500/MET500/TCA1000/THC50/BUP10/FYL1)+(AD1/AD2/AD3)+(AD4/AD5/AD6)

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

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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.