Omnicap
OMNIA SRL · Model 30.M0001.00 · UDI-DI 08056646507719
10
510(k) clearances
26
Adverse events
0
Recalls
294
Facilities
Description
Round cap with elastic - green
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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.