Vitex Biochemical products high sensitivity C-reactive protein reagent
Taiwan·Risk Class 2·ORTHO-CLINICAL DIAGNOSTICS, INC.·Registered Aug 09, 2017 – Aug 09, 2027Active- Analysis ID
- d84e7f1a674781190a4187d65cd50b7a
- Customs Code
- DHA05602982009
- Manufacturer
- ORTHO-CLINICAL DIAGNOSTICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- DKSH TAIWAN LTD.
- Intended Use
- This product is used with the Vitex 5,1FS/4600 chemical analyzer and the Vitex 5600 biochemical immunoassay analyzer to quantitatively detect C-reactive protein in serum and plasma.
- Product Type (Level 1)
- A Clinical Chemistry and Clinical Toxicology;; C Immunology and Microbiology
- Product Type (Level 2)
- A.1660 Grade Material (Analysis Material Non-Analysis);; A.1150 Calibrated Products;; C.5270 Canti-protein immunotry system
- Import Information
- import
- Registration Date
- Aug 09, 2017
- Expiry Date
- Aug 09, 2027
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Access comprehensive regulatory information for Vitex Biochemical products high sensitivity C-reactive protein reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d84e7f1a674781190a4187d65cd50b7a and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.. The authorized representative in Taiwan is DKSH TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC, and 1 recent registrations in the same category. 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.