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Rapid Response

BTNX Inc · Model D12.5.1-1V · UDI-DI 00722066004876

NGMNFWNGINGGPTGNFYNFVNGLPTHNFT
2
510(k) clearances
0
Adverse events
0
Recalls
40
Facilities

Description

One Step 12 Panel DOA Cup (12.5.1) - AMP500 BAR300 BUP10 BZO300 COC150 MDMA500 MTD300 MET500 MOP2000 OXY100 THC50 PCP25

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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.