NA
MEDICAL INSTRUMENT DEVELOPMENT LABORATORIES, INC. · Model 2405CE · UDI-DI 00812480010963
10
510(k) clearances
5
Adverse events
0
Recalls
5
Facilities
Description
20 Gauge Vitreous Cutter, SP, w/ 79” Posterior Tubing Set, Sterile, Extended Use
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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.