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"Randox" International Quality Assessment Scheme (RIQAS) (Non-Sterile) - Taiwan Registration 9a1d21499fb5f9ddc29fe1feb5ee3944

Access comprehensive regulatory information for "Randox" International Quality Assessment Scheme (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 9a1d21499fb5f9ddc29fe1feb5ee3944 and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is EUGENE-CHEN 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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9a1d21499fb5f9ddc29fe1feb5ee3944
Registration Details
Taiwan FDA Registration: 9a1d21499fb5f9ddc29fe1feb5ee3944
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Device Details

"Randox" International Quality Assessment Scheme (RIQAS) (Non-Sterile)
TW: "ๅ€ซๅคš" ๅœ‹้š›่ƒฝๅŠ›่ฉฆ้ฉ—่จˆ็•ซ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

9a1d21499fb5f9ddc29fe1feb5ee3944

Ministry of Health Medical Device Import No. 019081

DHA09401908101

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

May 23, 2018

May 23, 2028