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Shiji 5801 electrophoresis test kit - Taiwan Registration 4d51f83aca559a1d04b2f0bb3c8d91d3

Access comprehensive regulatory information for Shiji 5801 electrophoresis test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4d51f83aca559a1d04b2f0bb3c8d91d3 and manufactured by Shiji Biomedical Co., Ltd. Taipei Plant. The authorized representative in Taiwan is PHARMIGENE, INC..

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4d51f83aca559a1d04b2f0bb3c8d91d3
Registration Details
Taiwan FDA Registration: 4d51f83aca559a1d04b2f0bb3c8d91d3
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Device Details

Shiji 5801 electrophoresis test kit
TW: ไธ–ๅŸบ5801้›ปๆณณๆชขๆธฌๅฅ—็ต„
Risk Class 2
Cancelled

Registration Details

4d51f83aca559a1d04b2f0bb3c8d91d3

Company Information

Taiwan, Province of China

Product Details

The Shiji 5801 electrophoresis test set was used to qualitatively detect HLA-B*5801 gene by polymerase chain reaction technology.

A Clinical chemistry and clinical toxicology

A.3360 Genotype testing system for drug metabolic enzymes

Domestic

Dates and Status

Sep 18, 2012

Sep 18, 2022

Apr 12, 2024

Cancellation Information

Logged out

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