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"Zeiss" Laura Extended Astigmatism Correction of Hydrophilic Posterior Chamber Intraocular Lens - Taiwan Registration 35beea2426fa9ddee8899bc448ef106b

Access comprehensive regulatory information for "Zeiss" Laura Extended Astigmatism Correction of Hydrophilic 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 35beea2426fa9ddee8899bc448ef106b and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

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35beea2426fa9ddee8899bc448ef106b
Registration Details
Taiwan FDA Registration: 35beea2426fa9ddee8899bc448ef106b
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Device Details

"Zeiss" Laura Extended Astigmatism Correction of Hydrophilic Posterior Chamber Intraocular Lens
TW: โ€œ่”กๅธโ€่˜ฟๆ‹‰ๆ™ฏๆทฑๅปถ้•ทๆ•ฃๅ…‰็Ÿฏๆญฃ่ฆชๆฐดๆ€งๅพŒๆˆฟไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

35beea2426fa9ddee8899bc448ef106b

DHA05603447400

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

Mar 26, 2021

Mar 26, 2026