"Siemens" antithyroglobulin reagent group - Taiwan Registration fd43f62518ae84878630733a9b8a3ba2
Access comprehensive regulatory information for "Siemens" antithyroglobulin 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 fd43f62518ae84878630733a9b8a3ba2 and manufactured by 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.
Device Details
Product Details
This product is used for in vitro diagnostics, and needs to be used with ADVIA Centaur XP Systems, ADVIA Centaur XPT Systems, and ADVIA Centaur CP Systems to quantitatively detect thyroglobulin autoantibody content in serum or plasma.
A Clinical Chemistry and Clinical Toxicology;; C Immunology and Microbiology
C.5870 Cypress of the Upper Gland; A.1660 Grade Material (Analysis Material Non-Analysis);; A.1150 Calibrated Products
Input;; QMS/QSD
Dates and Status
Jun 17, 2022
Jun 17, 2027

