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“Sebia” Hypergamma Control - Taiwan Registration 19bb1573572847aaae8b1b6d0001e81a

Access comprehensive regulatory information for “Sebia” Hypergamma Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 19bb1573572847aaae8b1b6d0001e81a and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..

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19bb1573572847aaae8b1b6d0001e81a
Registration Details
Taiwan FDA Registration: 19bb1573572847aaae8b1b6d0001e81a
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Device Details

“Sebia” Hypergamma Control
TW: “賽比亞” 高濃度伽馬蛋白電泳品管液
Risk Class 2
MD

Registration Details

19bb1573572847aaae8b1b6d0001e81a

Ministry of Health Medical Device Import No. 029320

DHA05602932002

Company Information

France

Product Details

This product is used on HYDRAGEL, CAPILLARYS and MINICAP and other instruments as a quality control substance for human serum protein electrophoresis quantitative test.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Feb 07, 2017

Feb 07, 2027