Taiwan FDA registration 8c0daf2ef8ecfae64ca42cd3517952c6
BrightArt 1 Day Multifocal Silicone Hydrogel Soft Contact Lens
TW: 亮雅矽水膠漸進多焦點日拋軟性隱形眼鏡
Taiwan·Risk Class 2·MD·APEXLENS CO., LTD.·Registered Sep 13, 2022 – Sep 13, 2027ActiveRegistration details
- Analysis ID
- 8c0daf2ef8ecfae64ca42cd3517952c6
- License Form
- Ministry of Health Medical Device Manufacturing No. 007683
Company information
- Manufacturer
- APEXLENS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- APEXLENS CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M5925 Flexible Contact Lens
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 13, 2022
- Expiry Date
- Sep 13, 2027
About this record
Access comprehensive regulatory information for BrightArt 1 Day Multifocal Silicone Hydrogel Soft Contact Lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8c0daf2ef8ecfae64ca42cd3517952c6 and manufactured by APEXLENS CO., LTD.. The authorized representative in Taiwan is APEXLENS CO., LTD..
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