CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS Adverse Event — Injury (MDR 2015691-2020-11708)
CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS Adverse Event — Injury (MDR 2015691-2020-11708) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS; Generic name: REPLACEMENT HEART VALVE; Manufacturer: EDWARDS
| Device | CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS |
|---|---|
| Generic name | REPLACEMENT HEART VALVE |
| Manufacturer | EDWARDS LIFESCIENCES |
| Report number | 2015691-2020-11708 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | CORRECTED DATA: UPDATED SECTIONS B2 AND H6. |
| Source | openFDA MAUDE (device adverse events) |
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