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In.Pact™ 018

MEDTRONIC, INC. · Model IPU05004020P · UDI-DI 00763000291341

ONU Prescription
0
510(k) clearances
5,888
Adverse events (528 deaths)
1
Recalls
26
Facilities

Description

DCB 018 IPU05004020P D5.0 L040 UL0200

Recalls

DateFirmReason
2022-03-23Medtronic Vascular, Inc.Packaging for Balloon Catheters may be damaged resulting in loss of sterility.

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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.