Taiwan FDA registration d447749b85367da245415e4216335fb5
“DIESSE” CHORUS TOXOPLASMA IgG AVIDITY
TW: “迪雅仕” 可錄思 弓漿蟲IgG抗體親和力試劑組
Taiwan·Risk Class 2·MD·DIESSE DIAGNOSTICA SENESE S.P.A.·Registered Dec 04, 2014 – Dec 04, 2024ExpiredRegistration details
- Analysis ID
- d447749b85367da245415e4216335fb5
- License Form
- Ministry of Health Medical Device Import No. 026756
- Customs Code
- DHA05602675601
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 with the Chorus system to qualitatively detect anti-toxoplasmosis 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
- Dec 04, 2014
- Expiry Date
- Dec 04, 2024
About this record
Access comprehensive regulatory information for “DIESSE” CHORUS TOXOPLASMA IgG AVIDITY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d447749b85367da245415e4216335fb5 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..
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