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"Roche" VENTANA HE 600 Eosin (Non-Sterile) - Taiwan Registration 7f28f03866ab88f994f4e95a439d5f46

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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7f28f03866ab88f994f4e95a439d5f46
Registration Details
Taiwan FDA Registration: 7f28f03866ab88f994f4e95a439d5f46
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Device Details

"Roche" VENTANA HE 600 Eosin (Non-Sterile)
TW: "็พ…ๆฐ" ๅ‡กๅก”้‚ฃไผŠ็ด…ๆŸ“่‰ฒ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

7f28f03866ab88f994f4e95a439d5f46

Ministry of Health Medical Device Import Registration No. 016005

DHA08401600500

Company Information

United States

Product Details

Limited to the first grade identification range of dyes and chemical solution dyes (B.1850) of the management measures for medical devices.

B Hematology and pathology devices

B1850 Dyes and chemical solution dyes

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026

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