Taiwan FDA registration 6889dcc2db070ef9ca4922848deb5125
AURORA Daily disposable silicone hydrogel contact lens
TW: 歐若拉日拋矽水膠隱形眼鏡
Taiwan·Risk Class 2·MD·HOPE VISION CO., LTD.·Registered Jul 15, 2020 – Mar 12, 2024ExpiredRegistration details
- Analysis ID
- 6889dcc2db070ef9ca4922848deb5125
- License Form
- Ministry of Health Medical Device Manufacturing No. 006881
Company information
- Manufacturer
- HOPE VISION CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HOPE VISION CO., LTD.
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
- Jul 15, 2020
- Expiry Date
- Mar 12, 2024
About this record
Access comprehensive regulatory information for AURORA Daily disposable silicone hydrogel 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 6889dcc2db070ef9ca4922848deb5125 and manufactured by HOPE VISION CO., LTD.. The authorized representative in Taiwan is HOPE VISION CO., LTD..
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