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ELMED

ELMED INCORPORATED · Model 31940-22 · UDI-DI 00842180188679

NWW Prescription
0
510(k) clearances
66
Adverse events (1 deaths)
0
Recalls
59
Facilities

Description

9 Fr. (3.0 mm), 40cm, Biopsy Cup Forceps-Serrated, Flexible

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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.