MAUDE report
MAUDE report 58761: CARPENTIER EDWARDS PERIMOUNT PERICADIAL BIOPROSTHESIS
Death · received Dec 23, 1996 · BAXTER HEALTHCARE CORP. EDWARDS CVS DIV.
Key facts
| MDR report key | 58761 |
|---|---|
| Report number | 6000002-1996-00395 |
| Event type | Death |
| Brand name | CARPENTIER EDWARDS PERIMOUNT PERICADIAL BIOPROSTHESIS |
| Model number | 6900 |
| Manufacturer | BAXTER HEALTHCARE CORP. EDWARDS CVS DIV. |
| Product code | LWR |
| Device class | Class III |
| Date received by FDA | Dec 23, 1996 |
| Report date | Nov 27, 1996 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 10–99 MAUDE reports for this brand
- 1–9 Death reports for this brand
- 1–9 Injury reports for this brand
- Yes Adverse event flagged
- No Product problem flagged
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE medical device reports
MAUDE holds medical device reports (MDRs) of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by manufacturers, importers, user facilities and the public. A report alone does not establish that a device caused an event.
Source: U.S. Food and Drug Administration (FDA), MAUDE (Manufacturer and User Facility Device Experience) database · Source date: