MAUDE manufacturer profile
COVIDIEN · NIP
MAUDE profile for Stent, Superficial Femoral Artery
Key facts
| Manufacturer | COVIDIEN |
|---|---|
| Manufacturer group | COVIDIEN |
| Product code | NIP |
| Product code name | Stent, Superficial Femoral Artery |
At a glance
- 1,000+ MAUDE reports
- 10–99 Death reports
- 100–999 Injury reports
- 100–999 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Activation, Positioning or Separation Problem, No Clinical Signs, Symptoms or Conditions, No Consequences Or Impact To Patient, Material Deformation, Adverse Event Without Identified Device or Use Problem, Detachment of Device or Device Component, Fracture, Patient Problem/Medical Problem 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