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..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
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
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