"Siemens" creatinine reagent
Taiwan·Risk Class 2·RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.·Registered Jun 28, 2018 – Jun 28, 2028Active- Analysis ID
- 133e4529fa195bafcce129dabdeb461f
- Customs Code
- DHA05603130906
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- This product is used with Atellica CH Analyzer to quantitatively detect creatinine concentration in human serum, plasma (lithium heparin) and urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1255 2,3-Diphosphoglyceric acid test system
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Jun 28, 2018
- Expiry Date
- Jun 28, 2028
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Access comprehensive regulatory information for "Siemens" creatinine reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 133e4529fa195bafcce129dabdeb461f 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 SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD., 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.