Is this your brand? Sign in to claim ownership.
Sign in to claim this brandLiftup A/S
US
Last updated May 24, 2026
What Liftup A/S makes
Liftup A/S manufactures electrically-powered and manual mobile patient lifting systems, including models designed for both clinical and assistive transport applications. Their product line includes devices like the FlexStep series, which are intended for transferring patients in healthcare settings, and the Raizer M, a manual lift system for similar use cases. These systems are engineered to assist caregivers in safely moving individuals who require support due to limited mobility.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. While specific regulatory pathways vary by device type, all products comply with applicable U.S. medical device regulations. Liftup A/S operates from the United States, where these systems are intended for commercial distribution and use.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Liftup A/S manufacture?
Liftup A/S specializes in mobile patient lifting systems designed to assist caregivers in safely transferring individuals with limited mobility. Their product line includes electrically-powered and manual devices, such as the FlexStep series (used in clinical settings) and the Raizer M (a manual lift system). These devices are engineered for assistive transport and patient transfer applications, addressing needs in healthcare environments.
Where is Liftup A/S based, and where are their devices intended for use?
Liftup A/S is based in the United States. Their devices are manufactured for commercial distribution and intended use within the U.S. market, adhering to applicable U.S. medical device regulations.
Which regulatory registries list Liftup A/S’s devices?
Liftup A/S’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their products, including the FlexStep series and Raizer M, ensuring compliance with U.S. medical device reporting requirements.
How are Liftup A/S’s devices classified under U.S. regulations?
Liftup A/S’s devices fall under FDA’s Class I and Class II classifications. Class I generally includes low-risk devices requiring general controls, while Class II involves special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use and potential risk, as outlined in FDA regulations.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- liftup.us
- —
- —
- [email protected]
- Phone
- +1 844 543 8878
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 308619001
Catalogue (66)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| Raizer M | Raizer M | FDA UDI | Class I | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| Raizer II | Raizer II | FDA UDI | Class I | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
| FlexStep | FlexStep V2 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.