MAUDE manufacturer profile
A&E MEDICAL CORPORATION · LDF
MAUDE profile for Electrode, Pacemaker, Temporary
Key facts
| Manufacturer | A&E MEDICAL CORPORATION |
|---|---|
| Manufacturer group | A&E MEDICAL CORPORATION |
| Product code | LDF |
| Product code name | Electrode, Pacemaker, Temporary |
At a glance
- 10–99 MAUDE reports
- 1–9 Death reports
- 10–99 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Fracture, No Clinical Signs, Symptoms or Conditions, Material Frayed, Pacing Problem, Insufficient Information, Defibrillation/Stimulation Problem, Detachment of Device or Device Component, No Information 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