"Siemens" creatinine reagent
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Mar 11, 2009 – Mar 11, 2029Active- Analysis ID
- d692d7f737f86d2e65a1ead3090f57cf
- Customs Code
- DHA00601996204
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- Detection of creatinine concentrations in human serum, plasma, and urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1225 肌氨酸酐試驗系統(Creatininetestsystem)
- Import Information
- Contract manufacturing;; input
- Registration Date
- Mar 11, 2009
- Expiry Date
- Mar 11, 2029
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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 d692d7f737f86d2e65a1ead3090f57cf and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. 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.