MAUDE manufacturer profile
CORDIS US. CORP · KNQ
MAUDE profile for Dilator, Esophageal
Key facts
| Manufacturer | CORDIS US. CORP |
|---|---|
| Manufacturer group | CORDIS US CORP. |
| Product code | KNQ |
| Product code name | Dilator, Esophageal |
At a glance
- 10–99 MAUDE reports
- 1–9 Injury reports
- 10–99 Malfunction reports
- 1–9 Problems flagged by Orca1 signal analytics
- No Consequences Or Impact To Patient, Burst Container or Vessel, No Clinical Signs, Symptoms or Conditions, Difficult to Remove, Leak/Splash, Detachment Of Device Component, Deflation Problem, No Known Impact Or Consequence To Patient 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