MAUDE manufacturer profile
HANDI-MOVE NV · FSA
MAUDE profile for Lift, Patient, Non-Ac-Powered
Key facts
| Manufacturer | HANDI-MOVE NV |
|---|---|
| Manufacturer group | HANDI-MOVE NV |
| Product code | FSA |
| Product code name | Lift, Patient, Non-Ac-Powered |
At a glance
- 10–99 MAUDE reports
- 1–9 Death reports
- 10–99 Injury reports
- 1–9 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Device Handling Problem, Patient Problem/Medical Problem, Fall, Device Tipped Over, Use of Device Problem, Skin Discoloration, Respiratory Distress, Bone Fracture(s) 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