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"Roche" VENTANA HE 600 Hematoxylin (Non-Sterile) - Taiwan Registration 39223da3b6cf59870481cd1768ae2b37

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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39223da3b6cf59870481cd1768ae2b37
Registration Details
Taiwan FDA Registration: 39223da3b6cf59870481cd1768ae2b37
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Device Details

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

Registration Details

39223da3b6cf59870481cd1768ae2b37

Ministry of Health Medical Device Import No. 015972

DHA09401597200

Company Information

United States

Product Details

B Hematology and pathology devices

B1850 Dyes and chemical solution dyes

Imported from abroad

Dates and Status

Dec 15, 2015

Dec 15, 2025

Cancellation Information

Logged out

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