"Siemens" broad range of C-reactive protein reagents
Taiwan·Risk Class 2·RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.·Registered Jan 22, 2008 – Jan 22, 2028Active- Analysis ID
- 59b6d3fd579b7bf55ce4d712c3d485ff
- Customs Code
- DHA00601892404
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- For in vitro diagnostics. Quantitative determination of C-reactive protein in human serum and plasma on the ADVIA automated chemical analysis system.
- 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
- import
- Registration Date
- Jan 22, 2008
- Expiry Date
- Jan 22, 2028
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Access comprehensive regulatory information for "Siemens" broad range of C-reactive protein reagents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 59b6d3fd579b7bf55ce4d712c3d485ff and manufactured by RANDOX LABORATORIES LTD.;; 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 LIMITED;; 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.