MAUDE manufacturer profile
MPRI · DTB
MAUDE profile for Permanent Pacemaker Electrode
Key facts
| Manufacturer | MPRI |
|---|---|
| Manufacturer group | MPRI |
| Product code | DTB |
| Product code name | Permanent Pacemaker Electrode |
At a glance
- 1,000+ MAUDE reports
- 1,000+ Death reports
- 1,000+ Injury reports
- 1,000+ Malfunction reports
- 100–999 Problems flagged by Orca1 signal analytics
- No Clinical Signs, Symptoms or Conditions, Under-Sensing, No Known Impact Or Consequence To Patient, Over-Sensing, High Capture Threshold, Adverse Event Without Identified Device or Use Problem, Device Dislodged or Dislocated, Unspecified Infection 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