SEBIA CAPI 3 CDT (Non-Sterile) - Taiwan Registration cf4c6fe359ea47d046c7a89c3899e8a7
Access comprehensive regulatory information for SEBIA CAPI 3 CDT (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 cf4c6fe359ea47d046c7a89c3899e8a7 and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..
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Device Details
Registration Details
cf4c6fe359ea47d046c7a89c3899e8a7
Ministry of Health Medical Device Import No. 022251
DHA09402225107
Product Details
Limited to the first level identification range of the measures for the administration of medical devices "r-glutamyl transferase (GGT) and isoenzyme test system (A.1360)".
A Clinical chemistry and clinical toxicology
A1360 r-glutamyl transferase (GGT) and isoenzyme test system
Imported from abroad
Dates and Status
Jan 18, 2021
Jan 18, 2026