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AESCULAP
Aesculap AG · Model FK317R · UDI-DI 04038653166268
GEG
Prescription
10
510(k) clearances
39
Adverse events
0
Recalls
228
Facilities
Description
Raspatory, curved, 7 1/4", (185 mm), straight blade, sharp, peek handle, width: 3 mm, non-sterile, reusable
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
