EasyStand Evolv Medium Glider
Model Evolv Medium Glider
EasyStand Evolv Medium Glider is a device classified as Class I in the EU and Class II in the US made by Altimate Medical, Inc., registered in EUDAMED on 21 Oct 2026 (Basic UDI-DI 0858921006V3489), cleared under FDA 510(k) K062402 on 21 Sep 2006 and listed in FDA GUDID since 19 Sep 2016 (UDI-DI 10858921006048), active as of 24 Oct 2026.
Active
CE MDR 510(k)
Valid until
No date given
FDA recalls
None found
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0858921006V3489 10858921006048 | Date21 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number10858921006048 | Date19 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE GUDID | NumberK062402 | Date21 Sep 2006 | StatusActive |
Official records
- EUDAMED public site 0858921006V3489
- AccessGUDID record 10858921006048
- FDA 510(k) database K062402
Across registries
- EUDAMED Basic UDI-DI 0858921006V3489 registered 21 Oct 2026 Active
- FDA 510(k) K062402 decided 21 Sep 2006 Active
- FDA GUDID UDI-DI 10858921006048 listed 19 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K062402
- Listed FDA GUDID 10858921006048
- Registered EUDAMED 0858921006V3489
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- EasyStand Evolv Medium Glider EUDAMEDEasyStand GUDID
- Generic name
- Manual stander/exerciser
- Model / reference
- Evolv Medium Glider
- Primary DI / UDI-DI
- 10858921006048
- Basic UDI-DI
- 0858921006V3489
- 510(k) Number
- FDA product code
- INO
- EMDN code
- Y050202 Standing frames
- GMDN term
- Manual stander/exerciser
- Device class
- Class I EUDAMEDClass II GUDID
- Regulation number
- 890.3110
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class I | Class II |
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