MAUDE report
MAUDE report 10309: 3-WAY MANIFOLD
Death · received Oct 18, 1993 · PROCEDURE PRODUCTS
Key facts
| MDR report key | 10309 |
|---|---|
| Report number | 10309 |
| Event type | Death |
| Brand name | 3-WAY MANIFOLD |
| Manufacturer | PROCEDURE PRODUCTS |
| Product code | DTL |
| Device class | Class II |
| Date received by FDA | Oct 18, 1993 |
| Report date | Oct 12, 1993 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- 1–9 Death reports for this brand
- None Injury reports for this brand
- Yes 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: