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“MeVis” Veolity Digital Imaging system - Taiwan Registration e2732affe964c6b18bd20017b8d3ab4b

Access comprehensive regulatory information for “MeVis” Veolity Digital Imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e2732affe964c6b18bd20017b8d3ab4b and manufactured by MeVis Medical Solutions AG. The authorized representative in Taiwan is NAN KAI CORPORATION.

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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e2732affe964c6b18bd20017b8d3ab4b
Registration Details
Taiwan FDA Registration: e2732affe964c6b18bd20017b8d3ab4b
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Device Details

“MeVis” Veolity Digital Imaging system
TW: “優可視”影像輔助判讀系統
Risk Class 2
MD

Registration Details

e2732affe964c6b18bd20017b8d3ab4b

Ministry of Health Medical Device Import No. 035117

DHA05603511704

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P2050 Medical Image Management and Processing System

Imported from abroad

Dates and Status

Dec 16, 2021

Dec 16, 2026