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Blood Ketone Tester Set (Unsterilized) - Taiwan Registration 9629201e23cfb3d89c5f5b8ff6c0bf35

Access comprehensive regulatory information for Blood Ketone Tester Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9629201e23cfb3d89c5f5b8ff6c0bf35 and manufactured by Hsinchu General Factory of Weishi Biotechnology Co., Ltd. The authorized representative in Taiwan is Hsinchu General Factory of Weishi Biotechnology Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Hsinchu General Factory of Weishi Biotechnology Co., Ltd, and 1 recent registrations in the same category. 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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9629201e23cfb3d89c5f5b8ff6c0bf35
Registration Details
Taiwan FDA Registration: 9629201e23cfb3d89c5f5b8ff6c0bf35
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Device Details

Blood Ketone Tester Set (Unsterilized)
TW: ๆšไธ–่ก€้…ฎๆธฌ่ฉฆๅ„€ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

9629201e23cfb3d89c5f5b8ff6c0bf35

Company Information

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

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Oct 31, 2019

Oct 31, 2029

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