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Identify Diagnostics Multi-Drug Rapid Test Cup

Hangzhou AllTest Biotech Co., Ltd. · Model 1 · UDI-DI 16942598222000

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10
510(k) clearances
1
Adverse events
0
Recalls
58
Facilities

Description

25T, EN, non-CE, AMP1000/BAR300/BUP10/BZO300/COC300/MDMA500/MET1000/MOP300/MTD300/OXY100/PCP25/THC50+CRE/SG/PH

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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.