MAUDE manufacturer profile
ETHICON ENDO-SURGERY, LLC. · FDP
MAUDE profile for Apparatus, Pneumoperitoneum, Automatic
Key facts
| Manufacturer | ETHICON ENDO-SURGERY, LLC. |
|---|---|
| Manufacturer group | ETHICON ENDO-SURGERY, LLC. |
| Product code | FDP |
| Product code name | Apparatus, Pneumoperitoneum, Automatic |
At a glance
- 100–999 MAUDE reports
- 1–9 Death reports
- 1–9 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- No Clinical Signs, Symptoms or Conditions, Appropriate Term/Code Not Available, No Consequences Or Impact To Patient, Delivered as Unsterile Product, Retraction Problem, Device Operates Differently Than Expected, Patient Device Interaction Problem, Hemorrhage/Blood Loss/Bleeding 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