"Siemens" broad range of C-reactive protein reagents
Taiwan·Risk Class 2·RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Mar 30, 2021 – Mar 30, 2026Expired- Analysis ID
- 6eeaca24779099c4b282f0b64fb01a35
- Customs Code
- DHA05603438702
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- This product is used for in vitro diagnostic use and is used with Atellica CH Analyzer to quantitatively determine the concentration of C-reactive protein in human serum and plasma (heparin lithium).
- Product Type (Level 1)
- A Clinical Chemistry and Clinical Toxicology;; C Immunology and Microbiology
- Product Type (Level 2)
- A.1150 校正品;; C.5270 C反應蛋白免疫試驗系統
- Import Information
- QMS/QSD;; 輸入;; 委託製造
- Registration Date
- Mar 30, 2021
- Expiry Date
- Mar 30, 2026
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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 6eeaca24779099c4b282f0b64fb01a35 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.