"Siemens" ferritin reagent group
- Analysis ID
- df3989e6876553a016b31f1365aeae5f
- Customs Code
- DHA00601893904
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- Quantitative determination of ferritin 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.5880 運鐵蛋白免疫試驗系統
- Import Information
- import
- Registration Date
- Jan 24, 2008
- Expiry Date
- Jan 24, 2028
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Access comprehensive regulatory information for "Siemens" ferritin reagent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df3989e6876553a016b31f1365aeae5f 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 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.