Roche Vantana Magent-in-situ Hybridization Detection Tester (non-sterile) - Taiwan Registration e7e67b843233947c9ddd1748437ba35f
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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Device Details
Product Details
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.
B Hematology, pathology, and genetics
B.1860 Immunopathological histochemistry reagents and kits
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Sep 05, 2024
Sep 05, 2029