G-Eo
G-Eo is a Class II device made by Reha Technology AG, listed in FDA GUDID since 2 Jun 2019 (UDI-DI 07640174420032), registry data as of 21 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number07640174420032 | Date2 Jun 2019 | StatusListed |
Official records
- AccessGUDID record 07640174420032
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Treadmill/elliptical gait rehabilitation system
- Model / reference
- G-EO
- Primary DI / UDI-DI
- 07640174420032
- FDA product code
- IKK
- GMDN term
- Treadmill/elliptical gait rehabilitation system
- Device class
- Class II
- Regulation number
- 890.1925
- GUDID distribution status
- In Commercial Distribution
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