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"Roche" VENTANA Red ISH DIG Detection Kit (Non-Sterile) - Taiwan Registration ec56612ab7a3a81b75fadb3df951c768

Access comprehensive regulatory information for "Roche" VENTANA Red ISH DIG Detection Kit (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 ec56612ab7a3a81b75fadb3df951c768 and manufactured by VENTANA MEDICAL SYSTEMS, INC.. The authorized representative in Taiwan is ROCHE DIAGNOSTICS LTD..

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ec56612ab7a3a81b75fadb3df951c768
Registration Details
Taiwan FDA Registration: ec56612ab7a3a81b75fadb3df951c768
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Device Details

"Roche" VENTANA Red ISH DIG Detection Kit (Non-Sterile)
TW: "็พ…ๆฐ" ๅ‡กๅก”้‚ฃ็ด…่‰ฒๅŽŸไฝ้›œไบคDIGๅตๆธฌ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ec56612ab7a3a81b75fadb3df951c768

Ministry of Health Medical Device Import No. 022057

DHA09402205701

Company Information

United States

Product Details

Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.

B Hematology and pathology devices

B1860 Immunopathological histochemical reagents and kits

Imported from abroad

Dates and Status

Oct 23, 2020

Oct 23, 2025