Taiwan FDA registration cb8b66c4937509758f6f39850539b64c

“DIESSE” CHORUS TOXOPLASMA IgG

TW: “迪雅仕” 可錄思 弓漿蟲IgG抗體試劑組
Taiwan flagTaiwan·Risk Class 2·MD·DIESSE DIAGNOSTICA SENESE S.P.A.·Registered Oct 29, 2015 – Oct 29, 2025Expired
Registration details
Analysis ID
cb8b66c4937509758f6f39850539b64c
License Form
Ministry of Health Medical Device Import No. 027887
Customs Code
DHA05602788705
Company information
Manufacturer Country
Italy
Authorized Representative
GRAND MARQUIS CO., LTD.
Product details
Intended Use
This product is used with the Chorus system to quantitatively detect Toxoplasma IgG antibodies in human serum.
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C3780 Toxoplasma rodent serum reagent
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 29, 2015
Expiry Date
Oct 29, 2025
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About this record

Access comprehensive regulatory information for “DIESSE” CHORUS TOXOPLASMA IgG in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cb8b66c4937509758f6f39850539b64c and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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