Taiwan FDA registration d9be58bc5c71f9bf2afeb0b3a4df2808
Beifei Jia Cheng orthokeratology sheet
TW: 倍飛佳成角膜塑型片
Taiwan·Risk Class 3·BRIGHTEN OPTIX CORPORATION·Registered Jul 30, 2020 – Nov 29, 2026ActiveRegistration details
- Analysis ID
- d9be58bc5c71f9bf2afeb0b3a4df2808
Company information
- Manufacturer
- BRIGHTEN OPTIX CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BRIGHTEN OPTIX CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.5916 硬式透氣隱形眼鏡
- Import Information
- Domestic;; For ophthalmologist only (ophthalmologist's prescription required)
Dates and status
- Registration Date
- Jul 30, 2020
- Expiry Date
- Nov 29, 2026
About this record
Access comprehensive regulatory information for Beifei Jia Cheng orthokeratology sheet in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d9be58bc5c71f9bf2afeb0b3a4df2808 and manufactured by BRIGHTEN OPTIX CORPORATION. The authorized representative in Taiwan is BRIGHTEN OPTIX CORPORATION.
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