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"Retex" liquid cerebrospinal fluid quality tube fluid - Taiwan Registration 2afc0f45726e06d88b7f9c5dba159aba

Access comprehensive regulatory information for "Retex" liquid cerebrospinal fluid quality tube fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2afc0f45726e06d88b7f9c5dba159aba and manufactured by RANDOX LABORATORIES LTD. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..

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2afc0f45726e06d88b7f9c5dba159aba
Registration Details
Taiwan FDA Registration: 2afc0f45726e06d88b7f9c5dba159aba
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Device Details

"Retex" liquid cerebrospinal fluid quality tube fluid
TW: "็‘žๅพทๅฃซ" ๆถฒๆ…‹่…ฆ่„Š้ซ“ๆถฒๅ“็ฎกๆถฒ
Risk Class 2

Registration Details

2afc0f45726e06d88b7f9c5dba159aba

DHA05603565200

Company Information

United Kingdom

Product Details

This product is intended for in vitro diagnostic use, quality control of cerebrospinal fluid assay in clinical biochemical systems. This product can be used to monitor the accuracy and reproducibility of cerebrospinal fluid assays.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical)

Input;; QMS/QSD

Dates and Status

May 31, 2022

May 31, 2027