MAUDE manufacturer profile
MPRI · DTD
MAUDE profile for Pacemaker Lead Adaptor
Key facts
| Manufacturer | MPRI |
|---|---|
| Manufacturer group | MPRI |
| Product code | DTD |
| Product code name | Pacemaker Lead Adaptor |
At a glance
- 10–99 MAUDE reports
- 10–99 Injury reports
- 1–9 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Adverse Event Without Identified Device or Use Problem, Unspecified Infection, No Known Impact Or Consequence To Patient, No Clinical Signs, Symptoms or Conditions, High Capture Threshold, Pocket Erosion, Discomfort, Fever 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