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"ZEISS" hydrophobic posterior chamber intraocular lens - Taiwan Registration 467cd95b17adbb89da556d5faac528f5

Access comprehensive regulatory information for "ZEISS" 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 467cd95b17adbb89da556d5faac528f5 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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467cd95b17adbb89da556d5faac528f5
Registration Details
Taiwan FDA Registration: 467cd95b17adbb89da556d5faac528f5
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Device Details

"ZEISS" hydrophobic posterior chamber intraocular lens
TW: โ€œ่”กๅธโ€ ็–ๆฐดๆ€งๅพŒๆˆฟไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

467cd95b17adbb89da556d5faac528f5

DHA05603691307

Company Information

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M.3600 Artificial Crystal

Input;; Contract manufacturing

Dates and Status

Feb 01, 2024

Feb 01, 2029