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AESCULAP

Aesculap AG · Model DF083R · UDI-DI 04038653035106

EKJ Prescription
10
510(k) clearances
3
Adverse events
0
Recalls
103
Facilities

Description

Burnisher composite, 1/2" (165 mm), double ended, hexagonal handle

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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.