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"AIRUI" monolithic anti-ultraviolet hydrophobic acrylic posterior chamber intraocular lens - Taiwan Registration 559b010b20b2fce804ceebef5dc6d318

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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559b010b20b2fce804ceebef5dc6d318
Registration Details
Taiwan FDA Registration: 559b010b20b2fce804ceebef5dc6d318
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Device Details

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

Registration Details

559b010b20b2fce804ceebef5dc6d318

DHA00602368101

Company Information

France;;United States

Product Details

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

M Ophthalmology

M.3600 Artificial Crystal

Contract manufacturing;; input

Dates and Status

Jun 21, 2012

Jun 21, 2017

Dec 20, 2019

Cancellation Information

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