Taiwan FDA registration b35987926690cafc023eb6bc337368c2

Yibi Blood Ketone Tester Set (Non-Sterilized/Sterilized)

TW: 醫必血酮測試儀套組(未滅菌/滅菌)
Taiwan flagTaiwan·Risk Class 1·Hsinchu General Factory of Weishi Biotechnology Co., Ltd·Registered Jun 11, 2024 – Jun 11, 2029Active
Registration details
Analysis ID
b35987926690cafc023eb6bc337368c2
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
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.
Product Type (Level 1)
A Clinical Chemistry and Clinical Toxicology;; I General, Plastic Surgery and Dermatology
Product Type (Level 2)
A.1435 Ketone (non-quantitative) testing system;; I.4800 Manual instruments for general surgery
Import Information
國產;; QMS/QSD
Dates and status
Registration Date
Jun 11, 2024
Expiry Date
Jun 11, 2029
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About this record

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 b35987926690cafc023eb6bc337368c2 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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