MAUDE manufacturer profile
ABBOTT VASCULAR INC. · NIP
MAUDE profile for Stent, Superficial Femoral Artery
Key facts
| Manufacturer | ABBOTT VASCULAR INC. |
|---|---|
| Manufacturer group | ABBOTT VASCULAR, REG # 2024168 |
| 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
- No Clinical Signs, Symptoms or Conditions, Activation Failure, Material Separation, No Consequences Or Impact To Patient, Adverse Event Without Identified Device or Use Problem, Difficult to Remove, Improper or Incorrect Procedure or Method, Difficult or Delayed Activation 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