MAUDE report
MAUDE report 451: LIFEPORT VASCULAR ACCESS SYSTEM
Malfunction · received Apr 3, 1992 · STRATO MEDICAL CORPORATION
Key facts
| MDR report key | 451 |
|---|---|
| Report number | 451 |
| Event type | Malfunction |
| Brand name | LIFEPORT VASCULAR ACCESS SYSTEM |
| Model number | NI |
| Catalog number | LPS 2009 |
| Manufacturer | STRATO MEDICAL CORPORATION |
| Product code | GCB |
| Device class | Class I |
| PMA or 510(k) number | Device Exempt |
| Date received by FDA | Apr 3, 1992 |
| Report date | Mar 26, 1992 |
| Report source | Maude |
At a glance
- None Device problems coded
- 100–999 MAUDE reports for this product code
- 100–999 MAUDE reports for this brand
- 1–9 Death reports for this brand
- 100–999 Injury reports for this brand
- 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: