Taiwan FDA registration bd22a1ceafe07a9c1b49456eff3d768e
"POWER WELL" Limb orthosis (Non-Sterile)
TW: "保衛" 肢體裝具 (未滅菌)
Registration details
- Analysis ID
- bd22a1ceafe07a9c1b49456eff3d768e
- License Form
- Ministry of Health Medical Device Manufacturing No. 006869
Company information
- Manufacturer
- POWER WELL HEALTHCARE TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- POWER WELL HEALTHCARE TECHNOLOGY CO., LTD.
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 08, 2017
- Expiry Date
- Aug 08, 2022
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "POWER WELL" Limb orthosis (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bd22a1ceafe07a9c1b49456eff3d768e and manufactured by POWER WELL HEALTHCARE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is POWER WELL HEALTHCARE TECHNOLOGY CO., LTD..
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