MAUDE report
MAUDE report 16006: ARGON BLITT CENTRAL VENOUS CATHETER
Injury · received Jun 17, 1994 · ARGON MEDICAL CORP.
Key facts
| MDR report key | 16006 |
|---|---|
| Report number | 16006 |
| Event type | Injury |
| Brand name | ARGON BLITT CENTRAL VENOUS CATHETER |
| Model number | 14G6 |
| Catalog number | 497662 |
| Manufacturer | ARGON MEDICAL CORP. |
| Product code | DQO |
| Device class | Class II |
| Date received by FDA | Jun 17, 1994 |
| Report date | Jun 17, 1994 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- No 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: