Taiwan FDA registration 236d06563b2e69ffc6938ec548502ccc

“Randox” Ammonia Ethanol Control

TW: “瑞德士” 氨/酒精品管液

Taiwan·Risk Class 2·MD·RANDOX LABORATORIES LTD.·Registered Oct 01, 2018 – Oct 01, 2023Expired

Registration details

Analysis ID: 236d06563b2e69ffc6938ec548502ccc
License Form: Ministry of Health Medical Device Import No. 031486
Customs Code: DHA05603148602

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 fluid for the detection of ammonia and alcohol to monitor the precision and analytical deviation of the detection system.
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 01, 2018
Expiry Date: Oct 01, 2023

About this record

Access comprehensive regulatory information for “Randox” Ammonia Ethanol Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 236d06563b2e69ffc6938ec548502ccc and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..

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