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ORTHO

ORTHO-CLINICAL DIAGNOSTICS, INC. · Model MTS213784F · UDI-DI 10758750006014

KSZ Prescription
4
510(k) clearances
10,406
Adverse events (6 deaths)
0
Recalls
29
Facilities

Description

Ortho ProVue™ Refurbished

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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.