Taiwan FDA registration 1a01616b1ff266c6556224c71210e922

“Randox” Human Assayed Multi-Sera Control

TW: “瑞德士” 人類多重血清品管液

Taiwan·Risk Class 2·MD·RANDOX LABORATORIES LTD.·Registered Nov 06, 2018 – Nov 06, 2023Expired

Registration details

Analysis ID: 1a01616b1ff266c6556224c71210e922
License Form: Ministry of Health Medical Device Import No. 031779
Customs Code: DHA05603177904

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 in vitro diagnostics, as a quality control of diagnostic testing, suitable for accuracy monitoring.
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: Nov 06, 2018
Expiry Date: Nov 06, 2023

About this record

Access comprehensive regulatory information for “Randox” Human Assayed Multi-Sera Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a01616b1ff266c6556224c71210e922 and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..

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