MAUDE manufacturer profile
COVIDIEN AG JUAREZ (MMJ) · FFX
MAUDE profile for System, Gastrointestinal Motility (Electrical)
Key facts
| Manufacturer | COVIDIEN AG JUAREZ (MMJ) |
|---|---|
| Manufacturer group | COVIDIEN AG JUAREZ (MMJ) |
| Product code | FFX |
| Product code name | System, Gastrointestinal Motility (Electrical) |
At a glance
- 10–99 MAUDE reports
- 1–9 Injury reports
- 1–9 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Adverse Event Without Identified Device or Use Problem, Device Difficult to Program or Calibrate, No Clinical Signs, Symptoms or Conditions, Gradient Increase, Inadequacy of Device Shape and/or Size, Perforation of Esophagus, Pneumonia, Pneumothorax 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