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Epimed

EPIMED INTERNATIONAL, INC · Model 135-1735 · UDI-DI 00818788020956

MIA Prescription

510(k) clearances

227

Adverse events (1 deaths)

Recalls

Facilities

Description

Flexible Introducer Cannula w/ 17g x 3.5" Tuohy Metal Hub

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.