MAUDE manufacturer profile
CORDIS CORPORATION · NIQ
MAUDE profile for Coronary Drug-Eluting Stent
Key facts
| Manufacturer | CORDIS CORPORATION |
|---|---|
| Manufacturer group | CORDIS CORPORATION |
| Product code | NIQ |
| Product code name | Coronary Drug-Eluting Stent |
At a glance
- 100–999 MAUDE reports
- 100–999 Death reports
- 100–999 Injury reports
- 100–999 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Reocclusion, Adverse Event Without Identified Device or Use Problem, Occlusion Within Device, Thrombosis, Fracture, Myocardial Infarction, Death, No Code Available Most reported problems
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE manufacturer and product code profiles
Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.
Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1