MAUDE manufacturer profile
OSCOR INC · LDF
MAUDE profile for Electrode, Pacemaker, Temporary
Key facts
| Manufacturer | OSCOR INC |
|---|---|
| Manufacturer group | OSCOR INC. |
| Product code | LDF |
| Product code name | Electrode, Pacemaker, Temporary |
At a glance
- 10–99 MAUDE reports
- 1–9 Death reports
- 1–9 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- No Known Impact Or Consequence To Patient, Material Rupture, Complete Heart Block, Adverse Event Without Identified Device or Use Problem, Human-Device Interface Problem, No Pacing, Connection Problem, Pacing Problem 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