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"Zeiss" Lisa trifocal astigmatism corrects hydrophilic posterior chamber intraocular lenses - Taiwan Registration 3319a75e0b03de65e10b0bf9d84ae1ee

Access comprehensive regulatory information for "Zeiss" Lisa trifocal astigmatism corrects hydrophilic posterior chamber intraocular lenses in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3319a75e0b03de65e10b0bf9d84ae1ee 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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3319a75e0b03de65e10b0bf9d84ae1ee
Registration Details
Taiwan FDA Registration: 3319a75e0b03de65e10b0bf9d84ae1ee
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Device Details

"Zeiss" Lisa trifocal astigmatism corrects hydrophilic posterior chamber intraocular lenses
TW: โ€œ่”กๅธโ€้บ—่ŽŽไธ‰็„ฆ้ปžๆ•ฃๅ…‰็Ÿฏๆญฃ่ฆชๆฐดๆ€งๅพŒๆˆฟไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

3319a75e0b03de65e10b0bf9d84ae1ee

DHA05603511401

Company Information

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M.3600 Artificial Crystal

import

Dates and Status

Dec 16, 2021

Dec 16, 2026