MAUDE report
MAUDE report 44137: MITSUBISHI EXL-8
Malfunction · received Oct 23, 1996 · MITSUBISHI ELECTRIC CORP.
Key facts
| MDR report key | 44137 |
|---|---|
| Report number | 2523750-1996-00001 |
| Event type | Malfunction |
| Brand name | MITSUBISHI EXL-8 |
| Model number | EXL-8 |
| Catalog number | * |
| Manufacturer | MITSUBISHI ELECTRIC CORP. |
| Product code | IYE |
| Device class | Class II |
| Date received by FDA | Oct 23, 1996 |
| Report date | Oct 22, 1996 |
| Report source | Maude |
At a glance
- None Device problems coded
- No Adverse event flagged
- Yes 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: