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Resectoscopy sheath

SOPRO-COMEG GmbH · Model 195 040 540BC · UDI-DI 04059082008783

FDC
1
510(k) clearances
440
Adverse events (2 deaths)
0
Recalls
37
Facilities

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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.