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Uric Acid Tester Set (Unsterilized) - Taiwan Registration 9729a6f1211f0a16d4ffe213bed3b4ee

Access comprehensive regulatory information for Uric Acid 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 9729a6f1211f0a16d4ffe213bed3b4ee 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. 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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9729a6f1211f0a16d4ffe213bed3b4ee
Registration Details
Taiwan FDA Registration: 9729a6f1211f0a16d4ffe213bed3b4ee
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Device Details

Uric Acid Tester Set (Unsterilized)
TW: ๆšไธ–ๅฐฟ้…ธๆธฌ่ฉฆๅ„€ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

9729a6f1211f0a16d4ffe213bed3b4ee

Company Information

Product Details

Limited to the first level identification scope of the "uric acid test system (A.1775)" of the Measures for the Classification and Grading Management of Medical Devices.

A Clinical chemistry and clinical toxicology

A.1775 ๅฐฟ้…ธ่ฉฆ้ฉ—็ณป็ตฑ

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Aug 09, 2022

Aug 09, 2027