SEBIA CAPILLARYS CDT (Non-Sterile) - Taiwan Registration 2aeb51f8af57a151392221c278dfd72d
Access comprehensive regulatory information for SEBIA CAPILLARYS 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 2aeb51f8af57a151392221c278dfd72d and manufactured by SEBIA. The authorized representative in Taiwan is ARQon Medtech Co., Ltd..
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Device Details
Registration Details
2aeb51f8af57a151392221c278dfd72d
Ministry of Health Medical Device Import No. 022538
DHA09402253801
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
Apr 27, 2021
Apr 27, 2026

