"Siemens" creatinine reagent - Taiwan Registration d692d7f737f86d2e65a1ead3090f57cf
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.
Device Details
Registration Details
d692d7f737f86d2e65a1ead3090f57cf
DHA00601996204
Product Details
Detection of creatinine concentrations in human serum, plasma, and urine.
A Clinical chemistry and clinical toxicology
A.1225 ่ๆฐจ้ ธ้ ่ฉฆ้ฉ็ณป็ตฑ(Creatininetestsystem)
Contract manufacturing;; input
Dates and Status
Mar 11, 2009
Mar 11, 2029

