MAUDE report
MAUDE report 71679: PRESTIGE SI TABLE
Malfunction · received Feb 19, 1997 · GE MEDICAL SYSTEMS EUROPE
Key facts
| MDR report key | 71679 |
|---|---|
| Report number | 57331-1997-00009 |
| Event type | Malfunction |
| Brand name | PRESTIGE SI TABLE |
| Model number | 891501G273 |
| Manufacturer | GE MEDICAL SYSTEMS EUROPE |
| Product code | KXJ |
| Device class | Class II |
| Date received by FDA | Feb 19, 1997 |
| Report date | Feb 18, 1997 |
| 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
- 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: