Taiwan FDA registration fd78f42f179563e2526f9c6f5f9a2ad5

"Randox" RIQAS EQA Immunoassay Programmes (Non-Sterile)

TW: "瑞德士" 免疫分析院外品管計劃 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RANDOX LABORATORIES LTD.·Registered Oct 04, 2018 – Oct 04, 2023Expired
Registration details
Analysis ID
fd78f42f179563e2526f9c6f5f9a2ad5
License Form
Ministry of Health Medical Device Import No. 019677
Customs Code
DHA09401967705
Company information
Manufacturer Country
United Kingdom
Authorized Representative
KUO'S YUAN IN ENTERPRISE CO., LTD.
Product details
Intended Use
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.
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
Oct 04, 2018
Expiry Date
Oct 04, 2023
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Access comprehensive regulatory information for "Randox" RIQAS EQA Immunoassay Programmes (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 fd78f42f179563e2526f9c6f5f9a2ad5 and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..

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