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Rapid Response

BTNX Inc · Model D12.11.1-1VA · UDI-DI 00722066004906

NGL PTG NFY PTH NFW NFT NGG NFV DJG DNK DJR DIS LDJ DIO DKZ DJC JXM Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

One Step 12 Panel DOA Cup + Adulteration Test (12.11.1) - MOP300 OXY100 BZO300 MOP2000 MET500 AMP500 COC150 THC50 MDMA500 BUP10 BAR300 MTD300 + Cre/pH/Oxi

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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.