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禮雅尚 EB 病毒早期抗原 IgG 檢測試劑-品管液 - Taiwan Registration afa72a43cf6efeb8865b4a02c820e23e

Access comprehensive regulatory information for 禮雅尚 EB 病毒早期抗原 IgG 檢測試劑-品管液 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number afa72a43cf6efeb8865b4a02c820e23e and manufactured by DIASORIN ITALIA S.P.A.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..

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afa72a43cf6efeb8865b4a02c820e23e
Registration Details
Taiwan FDA Registration: afa72a43cf6efeb8865b4a02c820e23e
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Device Details

禮雅尚 EB 病毒早期抗原 IgG 檢測試劑-品管液
Risk Class 2

Registration Details

afa72a43cf6efeb8865b4a02c820e23e

DHA05603624505

Company Information

Italy

Product Details

This product (negative and positive) is used to confirm the efficacy of the Epstein-Barr Virus Early Antigen IgG Detection Reagent on the Liashan Chemical Cold Light Immunoassay Analyzer.

A Clinical chemistry and clinical toxicology

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

QMS/QSD;; 輸入

Dates and Status

Dec 25, 2023

Dec 25, 2028