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"AIRUI" anti-ultraviolet hydrophobic acrylic posterior chamber intraocular lens - Taiwan Registration 4c73f2bbcff09a249b41bb59aa00cff6

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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4c73f2bbcff09a249b41bb59aa00cff6
Registration Details
Taiwan FDA Registration: 4c73f2bbcff09a249b41bb59aa00cff6
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Device Details

"AIRUI" anti-ultraviolet hydrophobic acrylic posterior chamber intraocular lens
TW: โ€œๆ„›้Šณโ€ๆŠ—็ดซๅค–็ทš็–ๆฐดๆ€งไธ™็ƒฏ้…ธ่„‚ๅพŒๆˆฟไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3
Cancelled

Registration Details

4c73f2bbcff09a249b41bb59aa00cff6

DHA00602131808

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.3600 Artificial Crystal

Input;; Contract manufacturing

Dates and Status

Aug 17, 2010

Aug 17, 2015

Aug 13, 2018

Cancellation Information

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