MAUDE report
MAUDE report 16008: UNIVERSAL PERCUTANEOUS INDUCER TRAY-GUIDE WIRE, J WIRE
Death · received Jun 22, 1994 · ARGON MEDICAL CORP.
Key facts
| MDR report key | 16008 |
|---|---|
| Report number | 16008 |
| Event type | Death |
| Brand name | UNIVERSAL PERCUTANEOUS INDUCER TRAY-GUIDE WIRE, J WIRE |
| Model number | UNKNOWN |
| Catalog number | 500200 |
| Manufacturer | ARGON MEDICAL CORP. |
| Product code | DQX |
| Device class | Class II |
| Date received by FDA | Jun 22, 1994 |
| Report date | Jun 22, 1994 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 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: