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Veress Needle

UNIMAX MEDICAL SYSTEMS INC. · Model FVN112000 · UDI-DI 04714127862002

FHOHIF Prescription
1
510(k) clearances
81
Adverse events (2 deaths)
0
Recalls
40
Facilities

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Data 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.