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Rumex
RUMEX INTERNATIONAL CORP. · Model 20-1021 · UDI-DI 00840159907993
10
510(k) clearances
23
Adverse events
1
Recalls
122
Facilities
Description
LASEK Trephine 9.00 mm, Preset Depth 70 Microns, Length 120 mm, Round Titanium Handle
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-05-03 | Surgical Instrument Service And Savings, Inc. | The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch. |
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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.