FDA device listing
Ameriglide Stratos Vertical Platorm Lift,Harmar Highlander II Vertical Platform Lift,Highlander II VPLX0400 Vertical…
FDA device listing 1585780822 · HARMAR MOBILITY, LLC
Key facts
| Proprietary names | Ameriglide Stratos Vertical Platorm Lift,Harmar Highlander II Vertical Platform Lift,Highlander II VPLX0400 Vertical Platform Lift |
|---|---|
| Owner/operator | HARMAR MOBILITY, LLC |
| Owner/operator number | 9058576 |
| Product codes | PCE |
| Device names | PCE - Permanently Mounted Wheelchair Platform Lift |
| Device class | Class II |
| Classification regulations (21 CFR) | 890.3930 |
| Review panels | Physical Medicine |
| Registered establishments | HARMAR MOBILITY, LLC |
| Establishment registrations | 3004153586 |
| FEI numbers | 3004153586 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database