Taiwan FDA registration 43277d6f64a61760a55adf12b121322b
Aurora 1-Day Anti-UV Disposable Contact Lens
TW: 歐若拉淨透潤抗紫外線日拋隱形眼鏡
Taiwan·Risk Class 2·MD·I-SEE VISION TECHNOLOGY INC.·Registered Feb 18, 2021 – Apr 30, 2025ExpiredRegistration details
- Analysis ID
- 43277d6f64a61760a55adf12b121322b
- License Form
- Ministry of Health Medical Device Manufacturing No. 007027
Company information
- Manufacturer
- I-SEE VISION TECHNOLOGY INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- I-SEE VISION TECHNOLOGY 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
- Feb 18, 2021
- Expiry Date
- Apr 30, 2025
About this record
Access comprehensive regulatory information for Aurora 1-Day Anti-UV Disposable 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 43277d6f64a61760a55adf12b121322b and manufactured by I-SEE VISION TECHNOLOGY INC.. The authorized representative in Taiwan is I-SEE VISION TECHNOLOGY INC..
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