Taiwan FDA registration 5735fe2563dc40ef8bc0465f094a8bb5
Aurora 1 month blue light block contact lens
TW: 極光月拋濾藍光隱形眼鏡
Taiwan·Risk Class 2·MD·VIZIONFOCUS INC.·Registered Apr 29, 2021 – Apr 29, 2026ExpiredRegistration details
- Analysis ID
- 5735fe2563dc40ef8bc0465f094a8bb5
- License Form
- Ministry of Health Medical Device Manufacturing No. 007129
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
- Apr 29, 2021
- Expiry Date
- Apr 29, 2026
About this record
Access comprehensive regulatory information for Aurora 1 month blue light block 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 5735fe2563dc40ef8bc0465f094a8bb5 and manufactured by VIZIONFOCUS INC.. The authorized representative in Taiwan is VIZIONFOCUS INC..
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