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Yibi Blood Ketone Tester Set (Non-Sterilized/Sterilized) - Taiwan Registration c30dc977eb09a86eb10df6b90bbd5985

Access comprehensive regulatory information for Yibi Blood Ketone Tester Set (Non-Sterilized/Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c30dc977eb09a86eb10df6b90bbd5985 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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c30dc977eb09a86eb10df6b90bbd5985
Registration Details
Taiwan FDA Registration: c30dc977eb09a86eb10df6b90bbd5985
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Device Details

Yibi Blood Ketone Tester Set (Non-Sterilized/Sterilized)
TW: ้†ซๅฟ…่ก€้…ฎๆธฌ่ฉฆๅ„€ๅฅ—็ต„(ๆœชๆป…่Œ/ๆป…่Œ)
Risk Class 1

Registration Details

c30dc977eb09a86eb10df6b90bbd5985

Company Information

Product Details

It is limited to the classification and grading management measures of medical devices "Ketone (non-quantitative) test system (A.1435)" and "general surgical manual instruments (I.4800) The first level of identification range.

A Clinical Chemistry and Clinical Toxicology;; I General, Plastic Surgery and Dermatology

A.1435 Ketone (non-quantitative) testing system;; I.4800 Manual instruments for general surgery

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Jun 17, 2024

Jun 17, 2029

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