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"Randox" RIQAS (Non-Sterile) - Taiwan Registration d38fdc17c1618e24a40a5c18f47a2893

Access comprehensive regulatory information for "Randox" RIQAS (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 d38fdc17c1618e24a40a5c18f47a2893 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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d38fdc17c1618e24a40a5c18f47a2893
Registration Details
Taiwan FDA Registration: d38fdc17c1618e24a40a5c18f47a2893
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Device Details

"Randox" RIQAS (Non-Sterile)
TW: "็‘žๅพทๅฃซ" ๅœ‹้š›ๅ“็ฎก่ฉ•ไผฐ่ฉฆๅŠ‘(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d38fdc17c1618e24a40a5c18f47a2893

Ministry of Health Medical Device Import No. 019822

DHA09401982201

Company Information

United Kingdom

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

Nov 15, 2018

Nov 14, 2023