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“DIESSE” CHORUS CYTOMEGALOVIRUS IgM - Taiwan Registration fd843dffdf3f52cb74c1d71e30dc6d04

Access comprehensive regulatory information for “DIESSE” CHORUS CYTOMEGALOVIRUS IgM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd843dffdf3f52cb74c1d71e30dc6d04 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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fd843dffdf3f52cb74c1d71e30dc6d04
Registration Details
Taiwan FDA Registration: fd843dffdf3f52cb74c1d71e30dc6d04
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Device Details

“DIESSE” CHORUS CYTOMEGALOVIRUS IgM
TW: “迪雅仕” 可錄思 巨細胞病毒IgM抗體試劑組
Risk Class 2
MD

Registration Details

fd843dffdf3f52cb74c1d71e30dc6d04

Ministry of Health Medical Device Import No. 028283

DHA05602828304

Company Information

Product Details

This product is used in the Chorus system for the qualitative detection of anti-cytomegalovirus IgM antibodies in human serum.

C Immunology and microbiology devices

C3175 CMV serum reagent

Imported from abroad

Dates and Status

Mar 04, 2016

Mar 04, 2026