Taiwan FDA registration 559b010b20b2fce804ceebef5dc6d318

"AIRUI" monolithic anti-ultraviolet hydrophobic acrylic posterior chamber intraocular lens

TW: “愛銳”單片型抗紫外線疏水性丙烯酸脂後房人工水晶體
Taiwan flagTaiwan·Risk Class 3·AAREN SCIENTIFIC FRANCE;; AAREN SCIENTIFIC INC.·Registered Jun 21, 2012 – Jun 21, 2017Cancelled
Registration details
Analysis ID
559b010b20b2fce804ceebef5dc6d318
Customs Code
DHA00602368101
Company information
Manufacturer Country
France;;United States
Authorized Representative
SHIN SHENG PHARMACEUTICAL 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.3600 Artificial Crystal
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Jun 21, 2012
Expiry Date
Jun 21, 2017
Cancellation Date
Dec 20, 2019
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for "AIRUI" monolithic anti-ultraviolet hydrophobic acrylic posterior chamber 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 559b010b20b2fce804ceebef5dc6d318 and manufactured by AAREN SCIENTIFIC FRANCE;; AAREN SCIENTIFIC INC.. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL CO., LTD..

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