Taiwan FDA registration e2732affe964c6b18bd20017b8d3ab4b
“MeVis” Veolity Digital Imaging system
TW: “優可視”影像輔助判讀系統
Registration details
- Analysis ID
- e2732affe964c6b18bd20017b8d3ab4b
- License Form
- Ministry of Health Medical Device Import No. 035117
- Customs Code
- DHA05603511704
Company information
- Manufacturer
- MeVis Medical Solutions AG
- Manufacturer Country
- Germany
- Authorized Representative
- NAN KAI CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P2050 Medical Image Management and Processing System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 16, 2021
- Expiry Date
- Dec 16, 2026
About this record
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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