Taiwan FDA registration 3fcca7ae42c3ca718dd0d3c0d4c8f578

“DIESSE” CHORUS Jo-1

TW: “迪雅仕” 可錄思Jo-1抗體試劑組
Taiwan flagTaiwan·Risk Class 2·MD·DIESSE DIAGNOSTICA SENESE S.P.A.·Registered Jan 22, 2015 – Jan 22, 2025Expired
Registration details
Analysis ID
3fcca7ae42c3ca718dd0d3c0d4c8f578
License Form
Ministry of Health Medical Device Import No. 026852
Customs Code
DHA05602685207
Company information
Manufacturer Country
Italy
Authorized Representative
GRAND MARQUIS CO., LTD.
Product details
Intended Use
This product is used with the Chorus system to semi-quantitatively measure anti-Jo-1 antibodies in human serum using immunoenzyme methods.
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C5660 Multiple autologous antibody immunoassay system
Import Information
Imported from abroad
Dates and status
Registration Date
Jan 22, 2015
Expiry Date
Jan 22, 2025
About this record

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.

Free DatabasePowered by Pure Global AI89,000+ Devices