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AESCULAP

AESCULAP, INC. · Model MA706R · UDI-DI 04046964566431

KBA Prescription
0
510(k) clearances
1
Adverse events
0
Recalls
86
Facilities

Description

COTTLE Raspatory, downwards cutting, 8 1/4", (210 mm), non perforating, non-sterile, reusable

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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.