Taiwan FDA registration eefd18fed41a064b15777a00a2bbdd57
StrokeViewer Perfusion
TW: "識卓" 腦血流灌注分析軟體
Taiwan·Risk Class 2·MD·NICo-Lab B.V.·Registered Sep 02, 2023 – Sep 02, 2028ActiveRegistration details
- Analysis ID
- eefd18fed41a064b15777a00a2bbdd57
- License Form
- Ministry of Health Medical Device Import No. 036596
- Customs Code
- DHA05603659608
Company information
- Manufacturer
- NICo-Lab B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- Veritas Biomedical Co. Ltd.
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
- Sep 02, 2023
- Expiry Date
- Sep 02, 2028
About this record
Access comprehensive regulatory information for StrokeViewer Perfusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eefd18fed41a064b15777a00a2bbdd57 and manufactured by NICo-Lab B.V.. The authorized representative in Taiwan is Veritas Biomedical 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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