Taiwan FDA registration 002348ebe094c16d26496d55c0a73293

"Roche" Vantana in situ hybrid blue field test kit (unsterilized)

TW: “羅氏”凡塔那原位雜交藍視野檢測套組(未滅菌)

Taiwan·Risk Class 1·VENTANA MEDICAL SYSTEMS, INC.·Registered Sep 08, 2021 – Sep 08, 2026Active

Registration details

Analysis ID: 002348ebe094c16d26496d55c0a73293
Customs Code: DHA09402263907

Company information

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

Product details

Intended Use: Limit the classification and grading management of medical equipment "immunopathological histochemical reagents and sets (B.1860) the first level identification range.
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: Sep 08, 2021
Expiry Date: Sep 08, 2026

About this record

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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