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“Cepheid” Xpert Check - Taiwan Registration 744080f0f42e1e0bd2fc845865b4e7ad

Access comprehensive regulatory information for “Cepheid” Xpert Check in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 744080f0f42e1e0bd2fc845865b4e7ad and manufactured by CEPHEID. The authorized representative in Taiwan is PROGRESSIVE GROUP INC..

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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744080f0f42e1e0bd2fc845865b4e7ad
Registration Details
Taiwan FDA Registration: 744080f0f42e1e0bd2fc845865b4e7ad
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Device Details

“Cepheid” Xpert Check
TW: “賽沛”艾斯柏特儀器檢查組
Risk Class 2
MD

Registration Details

744080f0f42e1e0bd2fc845865b4e7ad

Ministry of Health Medical Device Import No. 032401

DHA05603240102

Company Information

United States

Product Details

This product is a system for inspection, verification and hardware testing of 6-color GeneXpert modules.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Apr 08, 2019

Apr 08, 2024