SYMPHONY Adverse Event — Death (MDR 1000165971-2020-00375)
SYMPHONY Adverse Event — Death (MDR 1000165971-2020-00375) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SYMPHONY; Generic name: PULSE GENERATOR, PERMANENT, IMPLANTABLE; Manufacturer: SORIN CRM.
| Device | SYMPHONY |
|---|---|
| Generic name | PULSE GENERATOR, PERMANENT, IMPLANTABLE |
| Manufacturer | SORIN CRM |
| Report number | 1000165971-2020-00375 |
| Event type | Death |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | THE SERIAL NUMBER OF THE SUBJECT PACEMAKER IS UNKNOWN. THE EXACT IMPLANTATION DATE IS UNKNOWN. |
| Source | openFDA MAUDE (device adverse events) |
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