Taiwan FDA registration 5cbc3854c4b938095b0d5a0ac082a366

“Randox” Liquid Cardiac Control

TW: “瑞德士” 液態心臟標記品管液
Taiwan flagTaiwan·Risk Class 2·MD·RANDOX LABORATORIES LTD.·Registered Aug 16, 2018 – Aug 16, 2023Expired
Registration details
Analysis ID
5cbc3854c4b938095b0d5a0ac082a366
License Form
Ministry of Health Medical Device Import No. 031425
Customs Code
DHA05603142508
Company information
Manufacturer Country
United Kingdom
Authorized Representative
KUO'S YUAN IN ENTERPRISE CO., LTD.
Product details
Intended Use
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.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A1660 Quality Control Materials (Analytical and Non-Analytical)
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 16, 2018
Expiry Date
Aug 16, 2023
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About this record

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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