Taiwan FDA registration c41bf6a0d864471102cb7be8120cc958
"EyePro" Corrective Spectacle Lens (Non-Sterile)
TW: "愛鉑" 矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·SUNDEX OPTICAL CO., LTD.·Registered Jul 19, 2018 – Jul 19, 2023ExpiredRegistration details
- Analysis ID
- c41bf6a0d864471102cb7be8120cc958
- License Form
- Ministry of Health Medical Device Manufacturing No. 007357
Company information
- Manufacturer
- SUNDEX OPTICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Chaoqun Optical Glasses Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5844 corrective lenses
- Import Information
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Jul 19, 2018
- Expiry Date
- Jul 19, 2023
About this record
Access comprehensive regulatory information for "EyePro" Corrective Spectacle Lens (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 c41bf6a0d864471102cb7be8120cc958 and manufactured by SUNDEX OPTICAL CO., LTD.. The authorized representative in Taiwan is Chaoqun Optical Glasses Co., Ltd.
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