MAUDE manufacturer profile
CORDIS CORPORATION · NIP
MAUDE profile for Stent, Superficial Femoral Artery
Key facts
| Manufacturer | CORDIS CORPORATION |
|---|---|
| Manufacturer group | CORDIS CORPORATION |
| Product code | NIP |
| Product code name | Stent, Superficial Femoral Artery |
At a glance
- 10–99 MAUDE reports
- 1–9 Death reports
- 10–99 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- No Clinical Signs, Symptoms or Conditions, Difficult or Delayed Positioning, Detachment of Device or Device Component, Difficult to Remove, Defective Component, Material Split, Cut or Torn, Loss of or Failure to Bond, Peeled/Delaminated 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