Taiwan FDA registration 2540465faa544118bf3e6d87bf718ee1
Ticon akira Daily Disposable Soft Contact Lens
TW: 帝康綺拉每日拋棄式隱形眼鏡
Taiwan·Risk Class 2·MD·Jingjing Optics Co., Ltd. Asia Pacific Factory·Registered Sep 01, 2016 – Nov 14, 2022ExpiredRegistration details
- Analysis ID
- 2540465faa544118bf3e6d87bf718ee1
- License Form
- Ministry of Health Medical Device Manufacturing No. 005434
Company information
- Manufacturer
- Jingjing Optics Co., Ltd. Asia Pacific Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ST. SHINE OPTICAL 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
- Sep 01, 2016
- Expiry Date
- Nov 14, 2022
About this record
Access comprehensive regulatory information for Ticon akira Daily Disposable Soft 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 2540465faa544118bf3e6d87bf718ee1 and manufactured by Jingjing Optics Co., Ltd. Asia Pacific Factory. The authorized representative in Taiwan is ST. SHINE OPTICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices