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“DIESSE” CHORUS dsDNA-G - Taiwan Registration a7148a4fd8a9612c4a54bc99e7d1dd62

Access comprehensive regulatory information for “DIESSE” CHORUS dsDNA-G in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a7148a4fd8a9612c4a54bc99e7d1dd62 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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a7148a4fd8a9612c4a54bc99e7d1dd62
Registration Details
Taiwan FDA Registration: a7148a4fd8a9612c4a54bc99e7d1dd62
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Device Details

“DIESSE” CHORUS dsDNA-G
TW: “迪雅仕” 可錄思 dsDNA-G抗體試劑組
Risk Class 2
MD

Registration Details

a7148a4fd8a9612c4a54bc99e7d1dd62

Ministry of Health Medical Device Import No. 026860

DHA05602686006

Company Information

Product Details

This product is used in conjunction with the Chorus System to quantitatively measure anti-dsDNA IgG antibodies in human serum using immunoenzyme methods.

C Immunology and microbiology devices

C5100 Antinuclear antibody immunoassay system

Imported from abroad

Dates and Status

Jan 22, 2015

Jan 22, 2025