MAUDE report
MAUDE report 9403: SORENSON TRANSPAC II
No Answer Provided · received Jul 18, 1994 · ABBOTT LABORATORIES (ABBOTT CRITICAL CARE SYSTEM)
Key facts
| MDR report key | 9403 |
|---|---|
| Report number | 9403 |
| Event type | No Answer Provided |
| Brand name | SORENSON TRANSPAC II |
| Catalog number | 42576-01 |
| Manufacturer | ABBOTT LABORATORIES (ABBOTT CRITICAL CARE SYSTEM) |
| Product code | DRS |
| Device class | Class II |
| Date received by FDA | Jul 18, 1994 |
| Report date | Jul 6, 1994 |
| 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: