Home › Joimax GmbH › Fibre optic cable
Fibre optic cable
Joimax GmbH · Model CSLC0348 · UDI-DI 04260744830561
FWF
Prescription
10
510(k) clearances
288
Adverse events
2
Recalls
50
Facilities
Description
joimax® Fiber Optic Cable
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) |
Query this across every FDA database — by API.
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.