Taiwan FDA registration c674865ed01d869cc012914bbaae804c
RêVIA Blue Light Barrier 1day contact lenses
TW: 蕾美抗藍光日拋隱形眼鏡
Taiwan·Risk Class 2·MD·VIZIONFOCUS INC.·Registered Dec 02, 2022 – Jun 01, 2027ActiveRegistration details
- Analysis ID
- c674865ed01d869cc012914bbaae804c
- License Form
- Ministry of Health Medical Device Manufacturing No. 007779
Company information
- Manufacturer
- VIZIONFOCUS INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- VIZIONFOCUS INC.
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
- Dec 02, 2022
- Expiry Date
- Jun 01, 2027
About this record
Access comprehensive regulatory information for RêVIA Blue Light Barrier 1day contact lenses in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c674865ed01d869cc012914bbaae804c and manufactured by VIZIONFOCUS INC.. The authorized representative in Taiwan is VIZIONFOCUS INC..
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