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"Roche" Vantana in situ hybrid blue field test kit (unsterilized) - Taiwan Registration 002348ebe094c16d26496d55c0a73293

Access comprehensive regulatory information for "Roche" Vantana in situ hybrid blue field test kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 002348ebe094c16d26496d55c0a73293 and manufactured by VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..

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002348ebe094c16d26496d55c0a73293
Registration Details
Taiwan FDA Registration: 002348ebe094c16d26496d55c0a73293
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Device Details

"Roche" Vantana in situ hybrid blue field test kit (unsterilized)
TW: โ€œ็พ…ๆฐโ€ๅ‡กๅก”้‚ฃๅŽŸไฝ้›œไบค่—่ฆ–้‡Žๆชขๆธฌๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

002348ebe094c16d26496d55c0a73293

DHA09402263907

Company Information

United States

Product Details

Limit the classification and grading management of medical equipment "immunopathological histochemical reagents and sets (B.1860) the first level identification range.

B Hematology, pathology, and genetics

B.1860 Immunopathological histochemistry reagents and kits

Input;; QMS/QSD

Dates and Status

Sep 08, 2021

Sep 08, 2026