Pure Global

S&G 0430 test kit - Taiwan Registration ae89f9acafc842a780fefaa332d7a06d

Access comprehensive regulatory information for S&G 0430 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 ae89f9acafc842a780fefaa332d7a06d 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
ae89f9acafc842a780fefaa332d7a06d
Registration Details
Taiwan FDA Registration: ae89f9acafc842a780fefaa332d7a06d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

S&G 0430 test kit
TW: ไธ–ๅŸบ0430ๆชขๆธฌๅฅ—็ต„
Risk Class 2

Registration Details

ae89f9acafc842a780fefaa332d7a06d

DHY00500302908

Company Information

Taiwan, Province of China

Product Details

The Shiji 0430 Nucleic Acid Molecular Detection Kit used real-time polymerase chain reaction technology to analyze the genotype of CYP2C9*2 c.430 C>T SNP in biological samples.

A Clinical chemistry and clinical toxicology

A.3360 Genotype testing system for drug metabolic enzymes

Domestic

Dates and Status

Feb 11, 2010

Feb 11, 2030