MAUDE manufacturer profile
DAVIS & GECK CARIBE LTD · LDF
MAUDE profile for Electrode, Pacemaker, Temporary
Key facts
| Manufacturer | DAVIS & GECK CARIBE LTD |
|---|---|
| Manufacturer group | DAVIS & GECK CARIBE LTD |
| 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
- Detachment of Device or Device Component, No Clinical Signs, Symptoms or Conditions, Insufficient Information, Break, Material Frayed, Adverse Event Without Identified Device or Use Problem, Cardiac Arrest 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