Taiwan FDA registration fe049e8da68f34d5eab813b7e37a1c6f

"Randox" Liquid Immunoassay Premium

TW: "瑞德士" 液態免疫分析品管液

Taiwan·Risk Class 2·MD·RANDOX LABORATORIES LTD.·Registered Mar 29, 2019 – Mar 29, 2024Expired

Registration details

Analysis ID: fe049e8da68f34d5eab813b7e37a1c6f
License Form: Ministry of Health Medical Device Import No. 032387
Customs Code: DHA05603238705

Company information

Manufacturer: RANDOX LABORATORIES LTD.
Manufacturer Country: United Kingdom
Authorized Representative: KUO'S YUAN IN ENTERPRISE CO., LTD.

Product details

Intended Use: This product is used as a quality control in the test procedure for the quantitative inspection of the analytes contained.
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: Mar 29, 2019
Expiry Date: Mar 29, 2024

About this record

Access comprehensive regulatory information for "Randox" Liquid Immunoassay Premium in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe049e8da68f34d5eab813b7e37a1c6f and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..

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