Taiwan FDA registration e7e67b843233947c9ddd1748437ba35f

Roche Vantana Magent-in-situ Hybridization Detection Tester (non-sterile)

TW: "羅氏" 凡塔那洋紅色原位雜交偵測試劑(未滅菌)

Taiwan·Risk Class 1·VENTANA MEDICAL SYSTEMS, INC.·Registered Sep 05, 2024 – Sep 05, 2029Active

Registration details

Analysis ID: e7e67b843233947c9ddd1748437ba35f
Customs Code: DHA09402359301

Company information

Manufacturer: VENTANA MEDICAL SYSTEMS, INC.
Manufacturer Country: United States
Authorized Representative: ROCHE DIAGNOSTICS LTD.

Product details

Intended Use: It is limited to the first level of identification scope of the "Immunopathological Histochemical Reagents and Sets (B.1860)" for the classification and grading management measures of medical devices.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.1860 Immunopathological histochemistry reagents and kits
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Sep 05, 2024
Expiry Date: Sep 05, 2029

About this record

Access comprehensive regulatory information for Roche Vantana Magent-in-situ Hybridization Detection Tester (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 e7e67b843233947c9ddd1748437ba35f and manufactured by VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..

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