“QCMD” EQA Programme (Non-Sterile) - Taiwan Registration e896ecd68b9ac67e3b95fca4d5ae60eb
Access comprehensive regulatory information for “QCMD” EQA Programme (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e896ecd68b9ac67e3b95fca4d5ae60eb and manufactured by Quality Control for Molecular Diagnostics (QCMD). The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE 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.
Device Details
Registration Details
e896ecd68b9ac67e3b95fca4d5ae60eb
Ministry of Health Medical Device Import No. 020982
DHA09402098200
Product Details
Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
A Clinical chemistry and clinical toxicology
A1660 Quality Control Materials (Analytical and Non-Analytical)
Imported from abroad
Dates and Status
Oct 25, 2019
Oct 25, 2024

