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“Randox” Liquid Cardiac Control - Taiwan Registration 5cbc3854c4b938095b0d5a0ac082a366

Access comprehensive regulatory information for “Randox” Liquid Cardiac Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5cbc3854c4b938095b0d5a0ac082a366 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, 1 companies making similar products including RANDOX LABORATORIES LTD., and 1 recent registrations in the same category. 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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5cbc3854c4b938095b0d5a0ac082a366
Registration Details
Taiwan FDA Registration: 5cbc3854c4b938095b0d5a0ac082a366
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Device Details

“Randox” Liquid Cardiac Control
TW: “瑞德士” 液態心臟標記品管液
Risk Class 2
MD

Registration Details

5cbc3854c4b938095b0d5a0ac082a366

Ministry of Health Medical Device Import No. 031425

DHA05603142508

Company Information

United Kingdom

Product Details

This product is used in vitro diagnosis as a quality control of CK-MB Mass, Diagoxin, D-Dimer, hsCRP, Myoglobin, NT-ProBNP, Troponin I and Troponin T and other cardiac marker test items in clinical biochemistry and immunity.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Aug 16, 2018

Aug 16, 2023

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