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“DIESSE” CHORUS RUBELLA IgG - Taiwan Registration aed5fe7302d982ab3d1dd65c7c582efc

Access comprehensive regulatory information for “DIESSE” CHORUS RUBELLA IgG in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aed5fe7302d982ab3d1dd65c7c582efc and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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aed5fe7302d982ab3d1dd65c7c582efc
Registration Details
Taiwan FDA Registration: aed5fe7302d982ab3d1dd65c7c582efc
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Device Details

“DIESSE” CHORUS RUBELLA IgG
TW: “迪雅仕” 可錄思德國麻疹病毒IgG抗體試劑組
Risk Class 2
MD

Registration Details

aed5fe7302d982ab3d1dd65c7c582efc

Ministry of Health Medical Device Import No. 028312

DHA05602831201

Company Information

Product Details

This product is used in the Chorus system to quantitatively detect German measles virus IgG antibodies in human serum.

C Immunology and microbiology devices

C3510 German measles virus serological reagent

Imported from abroad

Dates and Status

Mar 21, 2016

Mar 21, 2026