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Merit Medical®

Merit Medical Systems, Inc. · Model 00884450136799 · UDI-DI 00884450136799

OEX
0
510(k) clearances
17
Adverse events (1 deaths)
2
Recalls
17
Facilities

Recalls

DateFirmReason
2009-03-16Spectranetics CorporationCatheter outer jacket may split during use.
2008-10-15Spectranetics CorporationCatheter pouch was mislabeled with the wrong size.

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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.