SYNERGY Adverse Event — Malfunction (MDR 2134265-2020-04870)
SYNERGY Adverse Event — Malfunction (MDR 2134265-2020-04870) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SYNERGY; Generic name: BIODEGRADABLE POLYMER DRUG ELUTING CORONARY STENT SYSTEM; Manufacturer: BOSTON SCIENTIFIC CORPORATION.
| Device | SYNERGY |
|---|---|
| Generic name | BIODEGRADABLE POLYMER DRUG ELUTING CORONARY STENT SYSTEM |
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Report number | 2134265-2020-04870 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | DATE OF EVENT: USED (B)(6) 2020 AS THE CORRECT DATE WAS NOT PROVIDED. DEVICE IS A COMBINATION PRODUCT. |
| Source | openFDA MAUDE (device adverse events) |
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