MAUDE report
MAUDE report 4018: BLUE FLEXTIP MULTI-LUMEN CATHETER
Injury · received Jul 30, 1992 · ARROW INTERNATIONAL INC.
Key facts
| MDR report key | 4018 |
|---|---|
| Report number | 4018 |
| Event type | Injury |
| Brand name | BLUE FLEXTIP MULTI-LUMEN CATHETER |
| Model number | AK-14703 |
| Catalog number | AK-14703 |
| Manufacturer | ARROW INTERNATIONAL INC. |
| Product code | GBP |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Jul 30, 1992 |
| Report date | Dec 20, 1991 |
| 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: