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MD DrugScreen

Medical Disposables Corp · Model MDC-6135F · UDI-DI 00860007913167

QDO

510(k) clearances

Adverse events

Recalls

171

Facilities

Description

MDC-6135F CLIA WAIVED 13 Panel Cup w/Fen (AMP1000/BAR300/BUP10/BZO300/COC300/FEN300/MDMA500/ OPI300/MTD300/MET1000/OXY100/PCP25/THC50)

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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.