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AESCULAP

Aesculap AG · Model FF275R · UDI-DI 04038653065417

KAG Prescription
2
510(k) clearances
1
Adverse events
0
Recalls
29
Facilities

Description

EAR SPECULUM HOLDER

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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.