SEBIA CAPI 3 Urine (Non-Sterile) - Taiwan Registration f093f8d6043fd1dfa3ac0c21387e8b83
Access comprehensive regulatory information for SEBIA CAPI 3 Urine (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f093f8d6043fd1dfa3ac0c21387e8b83 and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..
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Device Details
Registration Details
f093f8d6043fd1dfa3ac0c21387e8b83
Ministry of Health Medical Device Import No. 020510
DHA09402051008
Product Details
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Protein (Chemical Separation Method) Test System (A.1630)".
A Clinical chemistry and clinical toxicology
A1630 Protein (Chemical Separation) Test System
Imported from abroad
Dates and Status
May 31, 2019
May 31, 2024