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AESCULAP

Aesculap AG · Model OP940 · UDI-DI 04046963903848

FSS Prescription
10
510(k) clearances
118
Adverse events
0
Recalls
38
Facilities

Description

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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.