MAUDE report
MAUDE report 7771
Malfunction · received Feb 4, 1994 · QUINTON
Key facts
| MDR report key | 7771 |
|---|---|
| Report number | 7771 |
| Event type | Malfunction |
| Model number | 36CM DUAL LUMEN |
| Catalog number | 17680-001 |
| Manufacturer | QUINTON |
| Date received by FDA | Feb 4, 1994 |
| Report date | Aug 16, 1993 |
| 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: