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“DIESSE” CHORUS Jo-1 - Taiwan Registration 3fcca7ae42c3ca718dd0d3c0d4c8f578

Access comprehensive regulatory information for “DIESSE” CHORUS Jo-1 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fcca7ae42c3ca718dd0d3c0d4c8f578 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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3fcca7ae42c3ca718dd0d3c0d4c8f578
Registration Details
Taiwan FDA Registration: 3fcca7ae42c3ca718dd0d3c0d4c8f578
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Device Details

“DIESSE” CHORUS Jo-1
TW: “迪雅仕” 可錄思Jo-1抗體試劑組
Risk Class 2
MD

Registration Details

3fcca7ae42c3ca718dd0d3c0d4c8f578

Ministry of Health Medical Device Import No. 026852

DHA05602685207

Company Information

Product Details

This product is used with the Chorus system to semi-quantitatively measure anti-Jo-1 antibodies in human serum using immunoenzyme methods.

C Immunology and microbiology devices

C5660 Multiple autologous antibody immunoassay system

Imported from abroad

Dates and Status

Jan 22, 2015

Jan 22, 2025