Taiwan FDA registration 266f87bc582e686386484f2c89159ab5

Blood Ketone Tester Set (Unsterilized)

TW: 暐世血酮測試儀套組(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Hsinchu General Factory of Weishi Biotechnology Co., Ltd·Registered May 10, 2019 – May 10, 2029Active
Registration details
Analysis ID
266f87bc582e686386484f2c89159ab5
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
Limited to the classification and grading management of medical equipment "Ketone (non-quantitative) test system (A.1435)" first level identification range.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1435 Ketone (non-quantitative) testing system
Import Information
國產;; QMS/QSD
Dates and status
Registration Date
May 10, 2019
Expiry Date
May 10, 2029
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About this record

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 266f87bc582e686386484f2c89159ab5 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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