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RELIANT BALLOON Adverse Event — Injury (MDR 9612164-2020-01701)

RELIANT BALLOON Adverse Event — Injury (MDR 9612164-2020-01701) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: RELIANT BALLOON; Generic name: CATHETER, PERCUTANEOUS; Manufacturer: MEDTRONIC IRELAND.

DeviceRELIANT BALLOON
Generic nameCATHETER, PERCUTANEOUS
ManufacturerMEDTRONIC IRELAND
Report number9612164-2020-01701
Event typeInjury
Product problemN
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, FOREIG
Narrative(B)(4). IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
SourceopenFDA MAUDE (device adverse events)

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