Taiwan FDA registration 5573a09b58fc8c725bacd3199fdfa089

"Jiaosheng" added visual vision energy and Youshi blue presbyopia correction flexible intraocular lens

TW: “嬌生”添視明視能及優視藍老花矯正軟式人工水晶體
Taiwan flagTaiwan·Risk Class 3·Johnson & Johnson Surgical Vision, Inc.;; AMO PUERTO RICO MANUFACTURING, INC.·Registered Jan 17, 2020 – Jan 17, 2030Active
Registration details
Analysis ID
5573a09b58fc8c725bacd3199fdfa089
Customs Code
DHA05603322306
Company information
Manufacturer Country
United States
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.3600 Artificial Crystal
Import Information
import
Dates and status
Registration Date
Jan 17, 2020
Expiry Date
Jan 17, 2030
About this record

Access comprehensive regulatory information for "Jiaosheng" added visual vision energy and Youshi blue presbyopia correction flexible 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 5573a09b58fc8c725bacd3199fdfa089 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).

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