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WOLVERINE CORONARY CUTTING BALLOON MONORAIL Adverse Event — Malfunction (MDR 2134265-2020-05732)

WOLVERINE CORONARY CUTTING BALLOON MONORAIL Adverse Event — Malfunction (MDR 2134265-2020-05732) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: WOLVERINE CORONARY CUTTING BALLOON MONORAIL; Generic name: CATHETER, PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PT; Manufacturer:

DeviceWOLVERINE CORONARY CUTTING BALLOON MONORAIL
Generic nameCATHETER, PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PT
ManufacturerBOSTON SCIENTIFIC CORPORATION
Report number2134265-2020-05732
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, DISTRI
Narrative(B)(6).
SourceopenFDA MAUDE (device adverse events)

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