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“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..

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e896ecd68b9ac67e3b95fca4d5ae60eb
Registration Details
Taiwan FDA Registration: e896ecd68b9ac67e3b95fca4d5ae60eb
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Device Details

“QCMD” EQA Programme (Non-Sterile)
TW: “康西恩”外部品管計劃(未滅菌)
Risk Class 1
MD

Registration Details

e896ecd68b9ac67e3b95fca4d5ae60eb

Ministry of Health Medical Device Import No. 020982

DHA09402098200

Company Information

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