MAUDE report
MAUDE report 37973: ARTERIAL POST W LUER LOCKS DW 480
Death · received Sep 10, 1996 · NMC MPD
Key facts
| MDR report key | 37973 |
|---|---|
| Report number | 8030665-1996-00267 |
| Event type | Death |
| Brand name | ARTERIAL POST W LUER LOCKS DW 480 |
| Catalog number | 1392167 |
| Manufacturer | NMC MPD |
| Product code | FJK |
| Device class | Class II |
| Date received by FDA | Sep 10, 1996 |
| Report date | Aug 22, 1996 |
| Report source | Maude |
At a glance
- None Device problems coded
- 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: