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Multi-Drug Rapid Test Panel (Urine)

Hangzhou AllTest Biotech Co., Ltd. · Model 1 · UDI-DI 16936983131640

NFTNGLNFYNFWNGGPTGNFVPTHNGM
10
510(k) clearances
2
Adverse events
0
Recalls
50
Facilities

Description

25T, FDA CLIA waived, MOP300/MDMA500/OXY100/PCP25/MET1000/MTD300/BAR300/COC300/BZO300/AMP1000/THC50/BUP10

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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.