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"Roche" VENTANA HE 600 Eosin (Non-Sterile) - Taiwan Registration 878ae8174657d5ce3c78d4a68c1d95ce

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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878ae8174657d5ce3c78d4a68c1d95ce
Registration Details
Taiwan FDA Registration: 878ae8174657d5ce3c78d4a68c1d95ce
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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
Cancelled

Registration Details

878ae8174657d5ce3c78d4a68c1d95ce

Ministry of Health Medical Device Import No. 016005

DHA09401600506

Company Information

United States

Product Details

B Hematology and pathology devices

B1850 Dyes and chemical solution dyes

Imported from abroad

Dates and Status

Dec 21, 2015

Dec 21, 2025

Cancellation Information

Logged out

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