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Badiek Rotavirus Test Reagent – Tube Fluid - Taiwan Registration dde9c430f61675ea9fa9d11f11ba99a9

Access comprehensive regulatory information for Badiek Rotavirus Test Reagent – Tube Fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dde9c430f61675ea9fa9d11f11ba99a9 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT 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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dde9c430f61675ea9fa9d11f11ba99a9
Registration Details
Taiwan FDA Registration: dde9c430f61675ea9fa9d11f11ba99a9
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Device Details

Badiek Rotavirus Test Reagent – Tube Fluid
TW: 巴迪鐵克輪狀病毒檢驗試劑–品管液
Risk Class 2

Registration Details

dde9c430f61675ea9fa9d11f11ba99a9

DHA05603567601

Company Information

Korea, Republic of

Product Details

This product is used for in vitro diagnostic use for quality management of rotavirus test reagents.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical)

QMS/QSD;; 輸入

Dates and Status

Jul 13, 2022

Jul 13, 2027