FlexTest LOHAS Blood Ketone Monitoring System (Unsterilized) - Taiwan Registration 7966b6091b580e8a02d16d0f9318b142
Access comprehensive regulatory information for FlexTest LOHAS Blood Ketone Monitoring System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7966b6091b580e8a02d16d0f9318b142 and manufactured by BIOPTIK TECHNOLOGY, INC.. The authorized representative in Taiwan is BIOPTIK TECHNOLOGY, INC..
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Device Details
Product Details
Limited to the classification and grading management of medical equipment "Ketone (non-quantitative) test system (A.1435)" first level identification range.
A Clinical chemistry and clinical toxicology
A.1435 Ketone (non-quantitative) testing system
ๅ็ข;; QMS/QSD
Dates and Status
Dec 08, 2021
Dec 08, 2026

