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BIS/BIS-40

Oscor Inc. · Model BIS/BIS-40 · UDI-DI 00836559003151

DTD Prescription
1
510(k) clearances
741
Adverse events (40 deaths)
0
Recalls
13
Facilities

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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.