MAUDE manufacturer profile
ABBOTT VASCULAR INC. · MAF
MAUDE profile for Stent, Coronary
Key facts
| Manufacturer | ABBOTT VASCULAR INC. |
|---|---|
| Manufacturer group | ABBOTT VASCULAR, REG # 3005718570 (P099) |
| Product code | MAF |
| Product code name | Stent, Coronary |
At a glance
- 1,000+ MAUDE reports
- 10–99 Death reports
- 1,000+ Injury reports
- 100–999 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Failure to Advance, No Clinical Signs, Symptoms or Conditions, No Consequences Or Impact To Patient, Patient-Device Incompatibility, Improper or Incorrect Procedure or Method, Material Separation, Adverse Event Without Identified Device or Use Problem, Device Dislodged or Dislocated 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