Taiwan FDA registration 931a79262a55c531280c04f8bee8db37
Roche uPath pathology image management software
TW: 羅氏uPath病理影像管理軟體
Registration details
- Analysis ID
- 931a79262a55c531280c04f8bee8db37
- Customs Code
- DHA05603491705
Company information
- Manufacturer
- VENTANA MEDICAL SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ROCHE DIAGNOSTICS LTD.
Product details
- Intended Use
- This product is designed to view, manage, and share digital histopathological slide scans.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.1860 Immunopathological histochemistry reagents and kits
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Nov 17, 2021
- Expiry Date
- Nov 17, 2026
About this record
Access comprehensive regulatory information for Roche uPath pathology image management software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 931a79262a55c531280c04f8bee8db37 and manufactured by VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS 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 DatabasePowered by Pure Global AI89,000+ Devices