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Medos International Sàrl · Model 3010-19-016 · UDI-DI 10705034561486
OLO
Prescription
10
510(k) clearances
20,634
Adverse events (13 deaths)
0
Recalls
383
Facilities
Description
NAVIGATION ENABLED INSTRUMENTS DUAL LEAD CANNULATED TAP 6MM
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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.