Taiwan FDA registration fd3ab1a633b0647c97b7a833e73629d9
“Keeogo” Powered Walking Assistance Device
TW: “啟而走”動力式下肢助行器
Taiwan·Risk Class 2·MD·WISTRON MEDICAL TECHNOLOGY CORPORATION·Registered Aug 19, 2020 – Aug 19, 2025ExpiredRegistration details
- Analysis ID
- fd3ab1a633b0647c97b7a833e73629d9
- License Form
- Ministry of Health Medical Device Manufacturing No. 006953
Company information
- Manufacturer
- WISTRON MEDICAL TECHNOLOGY CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WISTRON MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3480 powered lower extremity exoskeleton limb device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 19, 2020
- Expiry Date
- Aug 19, 2025
About this record
Access comprehensive regulatory information for “Keeogo” Powered Walking Assistance Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd3ab1a633b0647c97b7a833e73629d9 and manufactured by WISTRON MEDICAL TECHNOLOGY CORPORATION. The authorized representative in Taiwan is WISTRON MEDICAL TECHNOLOGY CORPORATION.
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