MAUDE manufacturer profile
NUMED, INC. · PNF
MAUDE profile for Aortic Stent
Key facts
| Manufacturer | NUMED, INC. |
|---|---|
| Manufacturer group | NUMED, INC. |
| Product code | PNF |
| Product code name | Aortic Stent |
At a glance
- 10–99 MAUDE reports
- 1–9 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- No Known Impact Or Consequence To Patient, No Clinical Signs, Symptoms or Conditions, Detachment of Device or Device Component, No Information, Detachment Of Device Component, No Apparent Adverse Event, Device Dislodged or Dislocated, Improper or Incorrect Procedure or Method 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