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“Randox” Human Assayed Multi-Sera Control - Taiwan Registration 1a01616b1ff266c6556224c71210e922

Access comprehensive regulatory information for “Randox” Human Assayed Multi-Sera Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a01616b1ff266c6556224c71210e922 and manufactured by RANDOX LABORATORIES LTD.. 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.

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1a01616b1ff266c6556224c71210e922
Registration Details
Taiwan FDA Registration: 1a01616b1ff266c6556224c71210e922
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Device Details

“Randox” Human Assayed Multi-Sera Control
TW: “瑞德士” 人類多重血清品管液
Risk Class 2
MD

Registration Details

1a01616b1ff266c6556224c71210e922

Ministry of Health Medical Device Import No. 031779

DHA05603177904

Company Information

United Kingdom

Product Details

This product is used in vitro diagnostics, as a quality control of diagnostic testing, suitable for accuracy monitoring.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Nov 06, 2018

Nov 06, 2023