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“DIESSE” CHORUS HERPES SIMPLEX 1+2 IgM - Taiwan Registration cfae3518bc9b516b595805b3d5d43084

Access comprehensive regulatory information for “DIESSE” CHORUS HERPES SIMPLEX 1+2 IgM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cfae3518bc9b516b595805b3d5d43084 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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cfae3518bc9b516b595805b3d5d43084
Registration Details
Taiwan FDA Registration: cfae3518bc9b516b595805b3d5d43084
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Device Details

“DIESSE” CHORUS HERPES SIMPLEX 1+2 IgM
TW: “迪雅仕” 可錄思 單純皰疹病毒Ⅰ+Ⅱ型IgM抗體試劑組
Risk Class 2
MD

Registration Details

cfae3518bc9b516b595805b3d5d43084

Ministry of Health Medical Device Import No. 028284

DHA05602828406

Company Information

Product Details

This product is used in the Chorus system for the qualitative detection of anti-herpes simplex virus type I.+II. IgM antibodies in human serum.

C Immunology and microbiology devices

C3305 Herpes simplex virus serum reagent

Imported from abroad

Dates and Status

Mar 04, 2016

Mar 04, 2026