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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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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7966b6091b580e8a02d16d0f9318b142
Registration Details
Taiwan FDA Registration: 7966b6091b580e8a02d16d0f9318b142
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Device Details

FlexTest LOHAS Blood Ketone Monitoring System (Unsterilized)
TW: ๆ˜“็ซ‹ๆธฌ ๆจ‚ๆดป ่ก€้…ฎ ็›ฃๆธฌ็ณป็ตฑ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

7966b6091b580e8a02d16d0f9318b142

Company Information

Taiwan, Province of China

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

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Dec 08, 2021

Dec 08, 2026