Taiwan FDA registration 4c73f2bbcff09a249b41bb59aa00cff6

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

TW: “愛銳”抗紫外線疏水性丙烯酸脂後房人工水晶體
Taiwan flagTaiwan·Risk Class 3·OII INTERNATIONAL FRANCE;; OPHTHALMIC INNOVATIONS INTERNATIONAL, INC.·Registered Aug 17, 2010 – Aug 17, 2015Cancelled
Registration details
Analysis ID
4c73f2bbcff09a249b41bb59aa00cff6
Customs Code
DHA00602131808
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
Input;; Contract manufacturing
Dates and status
Registration Date
Aug 17, 2010
Expiry Date
Aug 17, 2015
Cancellation Date
Aug 13, 2018
Cancellation information
Status
Logged out
Reason
未展延而逾期者
About this record

Access comprehensive regulatory information for "AIRUI" 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 4c73f2bbcff09a249b41bb59aa00cff6 and manufactured by OII INTERNATIONAL FRANCE;; OPHTHALMIC INNOVATIONS INTERNATIONAL, INC.. The authorized representative in Taiwan is SHIN SHENG PHARMACEUTICAL CO., LTD..

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