Taiwan FDA registration fd843dffdf3f52cb74c1d71e30dc6d04
“DIESSE” CHORUS CYTOMEGALOVIRUS IgM
TW: “迪雅仕” 可錄思 巨細胞病毒IgM抗體試劑組
Taiwan·Risk Class 2·MD·DIESSE DIAGNOSTICA SENESE S.P.A.·Registered Mar 04, 2016 – Mar 04, 2026ExpiredRegistration details
- Analysis ID
- fd843dffdf3f52cb74c1d71e30dc6d04
- License Form
- Ministry of Health Medical Device Import No. 028283
- Customs Code
- DHA05602828304
Company information
- Manufacturer
- DIESSE DIAGNOSTICA SENESE S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- GRAND MARQUIS CO., LTD.
Product details
- Intended Use
- This product is used in the Chorus system for the qualitative detection of anti-cytomegalovirus IgM antibodies in human serum.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3175 CMV serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 04, 2016
- Expiry Date
- Mar 04, 2026
About this record
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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