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:
| Device | WOLVERINE CORONARY CUTTING BALLOON MONORAIL |
|---|---|
| Generic name | CATHETER, PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PT |
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Report number | 2134265-2020-05732 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, DISTRI |
| Narrative | (B)(6). |
| Source | openFDA MAUDE (device adverse events) |
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