SEBIA MINICAP CDT (Non-Sterile) - Taiwan Registration f18b1171d865c33824172210c6a5ab6d
Access comprehensive regulatory information for SEBIA MINICAP 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 f18b1171d865c33824172210c6a5ab6d and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..
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Device Details
Registration Details
f18b1171d865c33824172210c6a5ab6d
Ministry of Health Medical Device Import No. 022252
DHA09402225209
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