Pure Global

“HUMANOPTICS” Acrylic Intraocular Lens Aspira-aXA - Taiwan Registration 28f770004016f75fbe240037d4fecf31

Access comprehensive regulatory information for “HUMANOPTICS” Acrylic Intraocular Lens Aspira-aXA in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 28f770004016f75fbe240037d4fecf31 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
28f770004016f75fbe240037d4fecf31
Registration Details
Taiwan FDA Registration: 28f770004016f75fbe240037d4fecf31
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“HUMANOPTICS” Acrylic Intraocular Lens Aspira-aXA
TW: “優眼光學”優視非球面人工水晶體
Risk Class 3
MD

Registration Details

28f770004016f75fbe240037d4fecf31

Ministry of Health Medical Device Import No. 034229

DHA05603422900

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

Dec 23, 2020

Dec 23, 2025