MAUDE manufacturer profile
CARDINAL HEALTH · DRX
MAUDE profile for Electrode, Electrocardiograph
Key facts
| Manufacturer | CARDINAL HEALTH |
|---|---|
| Manufacturer group | CARDINAL HEALTH |
| Product code | DRX |
| Product code name | Electrode, Electrocardiograph |
At a glance
- 10–99 MAUDE 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, Dyspnea, Shaking/Tremors, Nausea, Skin Inflammation/ Irritation, Failure to Read Input Signal, Loss of or Failure to Bond 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