MAUDE manufacturer profile
ST. JUDE MEDICAL HEA · LDF
MAUDE profile for Electrode, Pacemaker, Temporary
Key facts
| Manufacturer | ST. JUDE MEDICAL HEA |
|---|---|
| Manufacturer group | ST. JUDE MEDICAL |
| Product code | LDF |
| Product code name | Electrode, Pacemaker, Temporary |
At a glance
- 1–9 MAUDE reports
- 1–9 Death reports
- 1–9 Problems flagged by Orca1 signal analytics
- Adverse Event Without Identified Device or Use Problem, Cardiac Perforation 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