Taiwan FDA registration c53dd1e1f35fccd6cf96f879973c2513
clariti elite Silicone Hydrogel Contact Lenses
TW: 珂朗清明晰矽水膠月拋軟式隱形眼鏡
Registration details
- Analysis ID
- c53dd1e1f35fccd6cf96f879973c2513
- License Form
- Ministry of Health Medical Device Import No. 029963
- Customs Code
- DHA05602996305
Company information
- Manufacturer
- COOPERVISION MANUFACTURING LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- COOPERVISION (TAIWAN) 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
- Imported from abroad
Dates and status
- Registration Date
- Jul 12, 2017
- Expiry Date
- Jul 12, 2027
About this record
Access comprehensive regulatory information for clariti elite Silicone Hydrogel 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 c53dd1e1f35fccd6cf96f879973c2513 and manufactured by COOPERVISION MANUFACTURING LTD.. The authorized representative in Taiwan is COOPERVISION (TAIWAN) 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