"Siemens" high sensitivity C-reactive protein reagent
Taiwan·Risk Class 2·RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered May 31, 2012 – May 31, 2027Active- Analysis ID
- 84ad4741dabbc1fa0f596c3309381bce
- Customs Code
- DHA00602364102
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- Quantitatively determine C-reactive protein levels in human serum and plasma in combination with ADVIA 1200, ADVIA 1650/1800 or ADVIA 2400 chemical systems.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5270 C反應蛋白免疫試驗系統
- Import Information
- Contract manufacturing;; input
- Registration Date
- May 31, 2012
- Expiry Date
- May 31, 2027
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Access comprehensive regulatory information for "Siemens" 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 84ad4741dabbc1fa0f596c3309381bce and manufactured by RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RANDOX LABORATORIES LTD.;; Siemens Healthcare 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.