MAUDE manufacturer profile
CORDIS CORPORATION · MIH
MAUDE profile for System, Endovascular Graft, Aortic Aneurysm Treatment
Key facts
| Manufacturer | CORDIS CORPORATION |
|---|---|
| Manufacturer group | CORDIS CORPORATION |
| Product code | MIH |
| Product code name | System, Endovascular Graft, Aortic Aneurysm Treatment |
At a glance
- 100–999 MAUDE reports
- 10–99 Death reports
- 10–99 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Adverse Event Without Identified Device or Use Problem, No Clinical Signs, Symptoms or Conditions, Appropriate Term / Code Not Available, Detachment of Device or Device Component, Aneurysm, Thrombosis/Thrombus, Ruptured Aneurysm, Unspecified Vascular 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