Identity
- Trade Name
- G-EO FDA UDI
- Generic Name
- Treadmill/elliptical gait rehabilitation system FDA UDI
- Device Name
- Robotic-assisted gait trainer FDA UDI
- Model / Reference
- G-EO FDA UDI
- Description
- Robotic-assisted gait trainer FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07640174420032 FDA UDI
- FDA Product Code
- IKK FDA UDI
- GMDN Term
- Treadmill/elliptical gait rehabilitation system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.1925 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Treadmill/elliptical gait rehabilitation system
G-Eo by Reha Technology AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Treadmill/elliptical gait rehabilitation system.
- THERA-Trainer lyra — medica Medizintechnik GmbH · Class II
- LEXO — tyromotion GmbH · Class II
- OMEGO — tyromotion GmbH · Class I
- Morning Walk — CUREXO, Inc. · Class II
- G-EO System — Reha Technology AG · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Reha Technology AG
Sources (1)
- FDA UDI b166062b-875e-47c5-9bb5-0c8b4f2ffa12 33 fields · synced May 30, 2026