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FLEXCATH ADVANCE STEERABLE SHEATH Adverse Event — Malfunction (MDR 3002648230-2020-00246)

FLEXCATH ADVANCE STEERABLE SHEATH Adverse Event — Malfunction (MDR 3002648230-2020-00246) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: FLEXCATH ADVANCE STEERABLE SHEATH; Generic name: CATHETER, STEERABLE; Manufacturer: MEDTRONIC CRYOCATH LP.

DeviceFLEXCATH ADVANCE STEERABLE SHEATH
Generic nameCATHETER, STEERABLE
ManufacturerMEDTRONIC CRYOCATH LP
Report number3002648230-2020-00246
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, FOREIG
NarrativeIF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
SourceopenFDA MAUDE (device adverse events)

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