Taiwan FDA registration 878ae8174657d5ce3c78d4a68c1d95ce

"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 Dec 21, 2015 – Dec 21, 2025Cancelled
Registration details
Analysis ID
878ae8174657d5ce3c78d4a68c1d95ce
License Form
Ministry of Health Medical Device Import No. 016005
Customs Code
DHA09401600506
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 21, 2015
Expiry Date
Dec 21, 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 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 878ae8174657d5ce3c78d4a68c1d95ce 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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