Taiwan FDA registration ec56612ab7a3a81b75fadb3df951c768
"Roche" VENTANA Red ISH DIG Detection Kit (Non-Sterile)
TW: "羅氏" 凡塔那紅色原位雜交DIG偵測試劑 (未滅菌)
Taiwan·Risk Class 1·MD·VENTANA MEDICAL SYSTEMS, INC.·Registered Oct 23, 2020 – Oct 23, 2025ExpiredRegistration details
- Analysis ID
- ec56612ab7a3a81b75fadb3df951c768
- License Form
- Ministry of Health Medical Device Import No. 022057
- Customs Code
- DHA09402205701
Company information
- Manufacturer
- VENTANA MEDICAL SYSTEMS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ROCHE DIAGNOSTICS LTD.
Product details
- Intended Use
- Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B1860 Immunopathological histochemical reagents and kits
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 23, 2020
- Expiry Date
- Oct 23, 2025
About this record
Access comprehensive regulatory information for "Roche" VENTANA Red ISH DIG Detection Kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec56612ab7a3a81b75fadb3df951c768 and manufactured by VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..
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