Taiwan FDA registration 20852079afc21b6129d58e9d7d73c6ca
RêVIA Blue Light Barrier 1 Day Contact Lens
TW: 蕾美濾藍光日拋隱形眼鏡
Taiwan·Risk Class 2·MD·VIZIONFOCUS INC.·Registered Mar 23, 2021 – Dec 28, 2025ExpiredRegistration details
- Analysis ID
- 20852079afc21b6129d58e9d7d73c6ca
- License Form
- Ministry of Health Medical Device Manufacturing No. 007104
Company information
- Manufacturer
- VIZIONFOCUS INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- VIZIONFOCUS INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5925 Flexible Contact Lens
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 23, 2021
- Expiry Date
- Dec 28, 2025
About this record
Access comprehensive regulatory information for RêVIA Blue Light Barrier 1 Day 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 20852079afc21b6129d58e9d7d73c6ca and manufactured by VIZIONFOCUS INC.. The authorized representative in Taiwan is VIZIONFOCUS INC..
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