MAUDE manufacturer profile
COOK VANDERGRIFT INC. · DRE
MAUDE profile for Dilator, Vessel, For Percutaneous Catheterization
Key facts
| Manufacturer | COOK VANDERGRIFT INC. |
|---|---|
| Manufacturer group | COOK VANDERGRIFT INC. |
| Product code | DRE |
| Product code name | Dilator, Vessel, For Percutaneous Catheterization |
At a glance
- 100–999 MAUDE reports
- 10–99 Death reports
- 10–99 Injury reports
- 1–9 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Adverse Event Without Identified Device or Use Problem, Low Blood Pressure/ Hypotension, Great Vessel Perforation, Cardiac Tamponade, Pericardial Effusion, Cardiac Perforation, Perforation of Vessels, Tricuspid Valve Insufficiency/ Regurgitation 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