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Urethrotomy knife

SOPRO-COMEG GmbH · Model 195 120 001BC · UDI-DI 04059082009339

EZO
1
510(k) clearances
69
Adverse events
1
Recalls
37
Facilities

Recalls

DateFirmReason
2010-12-22Olympus America Inc.The device sterile package seal shows evidence of being breached or was breached

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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.