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AESCULAP

Aesculap AG · Model EO226R · UDI-DI 04038653041503

HFB Prescription
10
510(k) clearances
60
Adverse events
1
Recalls
164
Facilities

Description

MUSEUX Uterine Dressing Forceps, curved to side, 9 1/2", (240 mm), toothed (2x2), screw lock, non-sterile, reusable

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.

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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.