PROMUS PREMIER Adverse Event — Malfunction (MDR 2134265-2020-05729)
PROMUS PREMIER Adverse Event — Malfunction (MDR 2134265-2020-05729) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PROMUS PREMIER; Generic name: STENT, CORONARY, DRUG-ELUTING; Manufacturer: BOSTON SCIENTIFIC CORPORATION.
| Device | PROMUS PREMIER |
|---|---|
| Generic name | STENT, CORONARY, DRUG-ELUTING |
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Report number | 2134265-2020-05729 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, DISTRI |
| Narrative | DEVICE IS A COMBINATION PRODUCT. |
| Source | openFDA MAUDE (device adverse events) |
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