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Dermanson Müster Cardiac Troponin I Flex Reagent Set - Taiwan Registration 9794dc8feb72e074568da7ea1c1f1094

Access comprehensive regulatory information for Dermanson Müster Cardiac Troponin I Flex Reagent Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9794dc8feb72e074568da7ea1c1f1094 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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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9794dc8feb72e074568da7ea1c1f1094
Registration Details
Taiwan FDA Registration: 9794dc8feb72e074568da7ea1c1f1094
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Device Details

Dermanson Müster Cardiac Troponin I Flex Reagent Set
TW: 德曼遜敏斯特心肌肌鈣蛋白I弗列克斯試劑組
Risk Class 2
Cancelled

Registration Details

9794dc8feb72e074568da7ea1c1f1094

DHA00602274700

Company Information

United States

Product Details

This product is used with the Dimension Vista System to measure serum and plasma centrotroponin I concentrations.

A Clinical chemistry and clinical toxicology

A.1215 Creatine phosphokinase/creatine kinase or isoenzyme testing system

import

Dates and Status

Nov 25, 2011

Nov 25, 2016

Jul 31, 2018

Cancellation Information

Logged out

未展延而逾期者