Taiwan FDA registration de1151245143fa45cb09e25f7c03baf5
ProArt Silicone Hydrogel Daily Disposable Soft Contact Lenses
TW: 沛雅矽水膠日拋軟性隱形眼鏡
Taiwan·Risk Class 2·MD·APEXLENS CO., LTD.·Registered Jul 03, 2018 – Jul 03, 2028ActiveRegistration details
- Analysis ID
- de1151245143fa45cb09e25f7c03baf5
- License Form
- Ministry of Health Medical Device Manufacturing No. 006121
Company information
- Manufacturer
- APEXLENS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- APEXLENS 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 03, 2018
- Expiry Date
- Jul 03, 2028
About this record
Access comprehensive regulatory information for ProArt Silicone Hydrogel Daily Disposable Soft Contact Lenses in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number de1151245143fa45cb09e25f7c03baf5 and manufactured by APEXLENS CO., LTD.. The authorized representative in Taiwan is APEXLENS 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