MAUDE manufacturer profile
CORDIS CORPORATION · NIO
MAUDE profile for Stent, Iliac
Key facts
| Manufacturer | CORDIS CORPORATION |
|---|---|
| Manufacturer group | CORDIS US CORP. |
| Product code | NIO |
| Product code name | Stent, Iliac |
At a glance
- 100–999 MAUDE reports
- 10–99 Death reports
- 100–999 Injury reports
- 100–999 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Difficult or Delayed Positioning, No Consequences Or Impact To Patient, No Clinical Signs, Symptoms or Conditions, Adverse Event Without Identified Device or Use Problem, Reocclusion, Occlusion Within Device, Material Frayed, Detachment of Device or Device Component 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