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BioPlex 2200

BIO-RAD LABORATORIES, INC. · Model 12000650 · UDI-DI 03610520653012

GMQLIP
10
510(k) clearances
37
Adverse events
0
Recalls
17
Facilities

Description

BioPlex 2200 Syphilis Total & RPR Reagent Pack

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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.