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“HUMANOPTICS”Acrylic Intraocular Lens_Triva-aAY - Taiwan Registration 5522dd666405e1125edf62aec7c0706f

Access comprehensive regulatory information for “HUMANOPTICS”Acrylic Intraocular Lens_Triva-aAY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5522dd666405e1125edf62aec7c0706f and manufactured by HumanOptics Holding AG. The authorized representative in Taiwan is MEDBEST ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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5522dd666405e1125edf62aec7c0706f
Registration Details
Taiwan FDA Registration: 5522dd666405e1125edf62aec7c0706f
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Device Details

“HUMANOPTICS”Acrylic Intraocular Lens_Triva-aAY
TW: “優眼光學”亮視淡黃色三焦點非球面人工水晶體
Risk Class 3
MD

Registration Details

5522dd666405e1125edf62aec7c0706f

Ministry of Health Medical Device Import No. 035341

DHA05603534109

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

Imported from abroad

Dates and Status

Mar 31, 2022

Mar 31, 2027