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Olympus

OLYMPUS Winter & Ibe GmbH · Model A2891 · UDI-DI 04042761004442

FDC Prescription
1
510(k) clearances
442
Adverse events (2 deaths)
0
Recalls
37
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.