MAUDE report
MAUDE report 4380
No Answer Provided · received Jul 31, 1992 · COBE GAMBRO HOSPAL
Key facts
| MDR report key | 4380 |
|---|---|
| Report number | 4380 |
| Event type | No Answer Provided |
| Model number | AK-10 SYSTEM |
| Catalog number | BCM10-3003 |
| Manufacturer | COBE GAMBRO HOSPAL |
| Date received by FDA | Jul 31, 1992 |
| Report date | Jul 29, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 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: