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Rapid Response

BTNX Inc · Model D10.3.1-1V · UDI-DI 00722066004913

NFYNGLPTGNGMPTHNFTNFWNFVNGG
1
510(k) clearances
0
Adverse events
0
Recalls
52
Facilities

Description

10 Panel One Step DOA Cup(10.3.1) - COC150 AMP500 MET500 THC50 MOP2000 PCP25 BAR300 BZO300 MTD300 MDMA500

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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.