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"ZEISS" Lucian aspheric hydrophobic posterior chamber intraocular lens - Taiwan Registration 3b640a20c9a68ace3497752233f98940

Access comprehensive regulatory information for "ZEISS" Lucian aspheric hydrophobic 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 3b640a20c9a68ace3497752233f98940 and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec Production, LLC.. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

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3b640a20c9a68ace3497752233f98940
Registration Details
Taiwan FDA Registration: 3b640a20c9a68ace3497752233f98940
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Device Details

"ZEISS" Lucian aspheric hydrophobic posterior chamber intraocular lens
TW: โ€œ่”กๅธโ€ ้œฒ่ฅฟไบž้ž็ƒ้ข็–ๆฐดๆ€งๅพŒๆˆฟไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

3b640a20c9a68ace3497752233f98940

DHA05603691804

Company Information

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M.3600 Artificial Crystal

Contract manufacturing;; input

Dates and Status

Feb 05, 2024

Feb 05, 2029