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Conmed Corporation · Model 8272-16 · UDI-DI 10845854024898
FWF
Prescription
10
510(k) clearances
288
Adverse events
2
Recalls
50
Facilities
Description
3DHD OVERWEAR GLASSES (BOX OF 5)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-01-19 | Smith & Nephew, Inc Endoscopy Division | Surgical camera control units were not designed and manufactured to pass the IEC 60101 testing for electrical fast transients (EFT) |
| 2007-01-19 | Smith & Nephew, Inc Endoscopy Division | Surgical camera control units were not designed and manufactured to pass the IEC 60101 testing for electrical fast transients (EFT) |
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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.