Taiwan FDA registration 6d28d9e4e9b7c61478470bbbe6ec6596

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

TW: “愛銳”單片型抗紫外線親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 May 29, 2012 – May 29, 2017Cancelled
Registration details
Analysis ID
6d28d9e4e9b7c61478470bbbe6ec6596
Customs Code
DHA00602359403
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
May 29, 2012
Expiry Date
May 29, 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 hydrophilic 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 6d28d9e4e9b7c61478470bbbe6ec6596 and manufactured by AAREN SCIENTIFIC FRANCE;; AAREN SCIENTIFIC INC.. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL CO., LTD..

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