Taiwan FDA registration 5d1982741fcfb06fa55c2f5f567ccfb1

"Jiaosheng" added visual vision energy and Youshi blue presbyopia correction new easy load preloaded intraocular lens

TW: “嬌生”添視明視能及優視藍老花矯正新易載預載式人工水晶體
Taiwan flagTaiwan·Risk Class 3·Johnson & Johnson Surgical Vision, Inc.;; AMO Groningen B.V.·Registered Mar 18, 2022 – Mar 18, 2027Active
Registration details
Analysis ID
5d1982741fcfb06fa55c2f5f567ccfb1
Customs Code
DHA05603533705
Company information
Manufacturer Country
United States;;Netherlands
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.3600 Artificial Crystal
Import Information
import
Dates and status
Registration Date
Mar 18, 2022
Expiry Date
Mar 18, 2027
About this record

Access comprehensive regulatory information for "Jiaosheng" added visual vision energy and Youshi blue presbyopia correction new easy load preloaded 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 5d1982741fcfb06fa55c2f5f567ccfb1 and manufactured by Johnson & Johnson Surgical Vision, Inc.;; AMO Groningen B.V.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).

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