MAUDE manufacturer profile
CORDIS CORPORATION · LIT
MAUDE profile for Catheter, Angioplasty, Peripheral, Transluminal
Key facts
| Manufacturer | CORDIS CORPORATION |
|---|---|
| Manufacturer group | CORDIS US CORP. |
| Product code | LIT |
| Product code name | Catheter, Angioplasty, Peripheral, Transluminal |
At a glance
- 1,000+ MAUDE reports
- 1–9 Death reports
- 100–999 Injury reports
- 1,000+ Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Burst Container or Vessel, No Clinical Signs, Symptoms or Conditions, No Consequences Or Impact To Patient, Leak/Splash, Detachment of Device or Device Component, Difficult to Remove, Deflation Problem, Material Rupture 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