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V. Mueller
STERIS CORPORATION · Model GU4140 · UDI-DI 10885403050046
EZO
Prescription
5
510(k) clearances
69
Adverse events
1
Recalls
37
Facilities
Description
OTIS URETHROTOME STRAIGHT with3 GUIDE TIPS and 2 KNIFE BLADES IN CASE OVERALL LENGTH 11-3/4 inches30CM
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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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
