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Alltest Multi-Drug Test Cup (Urine)

Hangzhou AllTest Biotech Co., Ltd. · Model 1 · UDI-DI 16936983193020

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

Description

25T, FDA Clia Waived, MOP300/OXY100/COC300/MET1000/BZO300/AMP1000/BUP10+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.