MAUDE manufacturer profile
STOCKERT GMBH · DRF
MAUDE profile for Catheter, Electrode Recording, Or Probe, Electrode Recording
Key facts
| Manufacturer | STOCKERT GMBH |
|---|---|
| Manufacturer group | STOCKERT GMBH |
| Product code | DRF |
| Product code name | Catheter, Electrode Recording, Or Probe, Electrode Recording |
At a glance
- 100–999 MAUDE reports
- 10–99 Death reports
- 100–999 Injury reports
- 100–999 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Insufficient Information, Fistula, Partial thickness (Second Degree) Burn, Adverse Event Without Identified Device or Use Problem, No Known Impact Or Consequence To Patient, Device Operates Differently Than Expected, No Consequences Or Impact To Patient, Death 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