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MollRing Cutter Transection Device

Lemaitre Vascular, Inc. · Model 4200-42 · UDI-DI 00840663102716

DWX Prescription
1
510(k) clearances
10
Adverse events
0
Recalls
6
Facilities

Description

MollRing Cutter Transection Device, 7mm

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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.