MAUDE report
MAUDE report 43195: ARJO
Malfunction · received Sep 13, 1996 · ARJO MANUFACTURING CO.
Key facts
| MDR report key | 43195 |
|---|---|
| Report number | 1922538-1996-00095 |
| Event type | Malfunction |
| Brand name | ARJO |
| Model number | MBXXXX |
| Catalog number | 212026 |
| Manufacturer | ARJO MANUFACTURING CO. |
| Product code | FSA |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Sep 13, 1996 |
| Report date | Sep 13, 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: