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Rapid Response

BTNX Inc · Model D12.36-1P29-25 · UDI-DI 10722066005641

NFTNFWNGGNGLNFVPTHNGMPTGQBF Prescription
10
510(k) clearances
2
Adverse events
0
Recalls
50
Facilities

Description

12- Drug Test Panel - 25/kit (12.36) - AMP1000 BAR300 BZO300 COC300 MDMA500 MET1000 OPI2000 PCP25 THC50 MTD300 OXY100 PPX300. For the detection of drugs in human urine.

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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.