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“Medica” Creatine Kinase Reagent Kit - Taiwan Registration cfef8f9a58e0f0b90816b1f3ce080404

Access comprehensive regulatory information for “Medica” Creatine Kinase Reagent Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cfef8f9a58e0f0b90816b1f3ce080404 and manufactured by MEDICA CORPORATION. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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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cfef8f9a58e0f0b90816b1f3ce080404
Registration Details
Taiwan FDA Registration: cfef8f9a58e0f0b90816b1f3ce080404
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Device Details

“Medica” Creatine Kinase Reagent Kit
TW: “美麗佳” 肌酸激酶試劑
Risk Class 2
MD

Registration Details

cfef8f9a58e0f0b90816b1f3ce080404

Ministry of Health Medical Device Import No. 025934

DHA05602593404

Company Information

United States

Product Details

This product is used with "Meijia" automatic biochemical analyzer to quantitatively detect creatine kinase in human serum.

A Clinical chemistry and clinical toxicology

A1225 Creatinine Test System

Imported from abroad

Dates and Status

Apr 03, 2014

Apr 03, 2024