"Siemens" creatinine reagent - Taiwan Registration 133e4529fa195bafcce129dabdeb461f
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.
Device Details
Registration Details
133e4529fa195bafcce129dabdeb461f
DHA05603130906
Product Details
This product is used with Atellica CH Analyzer to quantitatively detect creatinine concentration in human serum, plasma (lithium heparin) and urine.
A Clinical chemistry and clinical toxicology
A.1255 2,3-Diphosphoglyceric acid test system
Input;; Contract manufacturing
Dates and Status
Jun 28, 2018
Jun 28, 2028