Taiwan FDA registration 363c8ddd232f3baee8e5e751d861a8ab
"Kubai" bi-weekly soft contact lenses
TW: “酷柏”佰美視雙週拋軟式隱形眼鏡
Taiwan·Risk Class 2·COOPERVISION Manufacturing Puerto Rico, LLC·Registered Jun 24, 2011 – Jun 24, 2026ExpiredRegistration details
- Analysis ID
- 363c8ddd232f3baee8e5e751d861a8ab
- Customs Code
- DHA00602256800
Company information
- Manufacturer
- COOPERVISION Manufacturing Puerto Rico, LLC
- Manufacturer Country
- United States
- 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 Ophthalmology
- Product Type (Level 2)
- M.5925 軟式隱形眼鏡
- Import Information
- import
Dates and status
- Registration Date
- Jun 24, 2011
- Expiry Date
- Jun 24, 2026
About this record
Access comprehensive regulatory information for "Kubai" bi-weekly 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 363c8ddd232f3baee8e5e751d861a8ab and manufactured by COOPERVISION Manufacturing Puerto Rico, LLC. 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