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E-LINE
Richard Wolf GmbH · Model 8667111 · UDI-DI 04055207019207
5
510(k) clearances
69
Adverse events
1
Recalls
37
Facilities
Description
OBTURATOR FOR URETHROTOME 20.5FR WL 231 mm, oval, cannulated, rounded distal end, compatible with sheath 8667.011, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-12-22 | Olympus America Inc. | The device sterile package seal shows evidence of being breached or was breached |
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Get your free API keyRead the docsData 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.