MAUDE report
MAUDE report 58974: MAMMO DIAGNOST UM
Malfunction · received Dec 20, 1996 · PHILIPS SYSTEME MEDEZIN
Key facts
| MDR report key | 58974 |
|---|---|
| Report number | 1217116-1996-00034 |
| Event type | Malfunction |
| Brand name | MAMMO DIAGNOST UM |
| Model number | 9871-400-36012 |
| Manufacturer | PHILIPS SYSTEME MEDEZIN |
| Product code | IZH |
| Device class | Class II |
| Date received by FDA | Dec 20, 1996 |
| Report date | Nov 25, 1996 |
| Report source | Maude |
At a glance
- None Device problems coded
- 100–999 MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- None 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: