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“HUMANOPTICS” Acrylic Intraocular Lens_Aspira-aAY - Taiwan Registration fd1528cba4e8f568564fbc0ffd659ba3

Access comprehensive regulatory information for “HUMANOPTICS” Acrylic Intraocular Lens_Aspira-aAY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fd1528cba4e8f568564fbc0ffd659ba3 and manufactured by HumanOptics Holding AG. The authorized representative in Taiwan is MEDBEST ENTERPRISE CO., LTD..

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Registration Details
Taiwan FDA Registration: fd1528cba4e8f568564fbc0ffd659ba3
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Device Details

“HUMANOPTICS” Acrylic Intraocular Lens_Aspira-aAY
TW: “優眼光學”亮視淡黃色非球面人工水晶體
Risk Class 3
MD

Registration Details

fd1528cba4e8f568564fbc0ffd659ba3

Ministry of Health Medical Device Import No. 033896

DHA05603389605

Company Information

Germany

Product Details

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

M Ophthalmic devices

M3600 intraocular lens

Imported from abroad

Dates and Status

Aug 24, 2020

Aug 24, 2025