"Jiaosheng" Tian Shiming second-generation astigmatism correction monolithic folded intraocular lens
Taiwan·Risk Class 3·Johnson & Johnson Surgical Vision, Inc.;; AMO PUERTO RICO MANUFACTURING, INC.·Registered Jan 06, 2021 – Jan 06, 2026Expired- Analysis ID
- 8e74107d91a8c439cc2ba58030deb90e
- Customs Code
- DHA05603424100
- Manufacturer Country
- United States
- Authorized Representative
- AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG)
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3600 Artificial Crystal
- Import Information
- import
- Registration Date
- Jan 06, 2021
- Expiry Date
- Jan 06, 2026
Access comprehensive regulatory information for "Jiaosheng" Tian Shiming second-generation astigmatism correction monolithic folded intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8e74107d91a8c439cc2ba58030deb90e and manufactured by Johnson & Johnson Surgical Vision, Inc.;; AMO PUERTO RICO MANUFACTURING, INC.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).
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.