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"Siemens" antithyroglobulin reagent group - Taiwan Registration 2e97ddd4c67cd4cf3743018000b07813

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 2e97ddd4c67cd4cf3743018000b07813 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.

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2e97ddd4c67cd4cf3743018000b07813
Registration Details
Taiwan FDA Registration: 2e97ddd4c67cd4cf3743018000b07813
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Device Details

"Siemens" antithyroglobulin reagent group
TW: โ€œ่ฅฟ้–€ๅญโ€ ๆŠ—็”ฒ็‹€่…บ็ƒ่›‹็™ฝ่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

2e97ddd4c67cd4cf3743018000b07813

DHA05603204901

Company Information

United States

Product Details

This product is used with Atellica IM Analyzer to quantitatively detect thyroglobulin autoantibodies in human serum and plasma (EDTA).

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

import

Dates and Status

Jan 14, 2019

Jan 14, 2029

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