Taiwan FDA registration 7f28f03866ab88f994f4e95a439d5f46

"Roche" VENTANA HE 600 Eosin (Non-Sterile)

TW: "羅氏" 凡塔那伊紅染色試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·VENTANA MEDICAL SYSTEMS, INC.·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
7f28f03866ab88f994f4e95a439d5f46
License Form
Ministry of Health Medical Device Import Registration No. 016005
Customs Code
DHA08401600500
Company information
Manufacturer Country
United States
Authorized Representative
ROCHE DIAGNOSTICS LTD.
Product details
Intended Use
Limited to the first grade identification range of dyes and chemical solution dyes (B.1850) of the management measures for medical devices.
Product Type (Level 1)
B Hematology and pathology devices
Product Type (Level 2)
B1850 Dyes and chemical solution dyes
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

Access comprehensive regulatory information for "Roche" VENTANA HE 600 Eosin (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 7f28f03866ab88f994f4e95a439d5f46 and manufactured by VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including VENTANA MEDICAL SYSTEMS, INC., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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