Taiwan FDA registration 39223da3b6cf59870481cd1768ae2b37

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

TW: "羅氏" 凡塔那蘇木素染色試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·VENTANA MEDICAL SYSTEMS, INC.·Registered Dec 15, 2015 – Dec 15, 2025Cancelled
Registration details
Analysis ID
39223da3b6cf59870481cd1768ae2b37
License Form
Ministry of Health Medical Device Import No. 015972
Customs Code
DHA09401597200
Company information
Manufacturer Country
United States
Authorized Representative
ROCHE DIAGNOSTICS LTD.
Product details
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
Dec 15, 2015
Expiry Date
Dec 15, 2025
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Roche" VENTANA HE 600 Hematoxylin (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 39223da3b6cf59870481cd1768ae2b37 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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