Blood Ketone Tester Set (Unsterilized)
- Analysis ID
- 9629201e23cfb3d89c5f5b8ff6c0bf35
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Hsinchu General Factory of Weishi Biotechnology Co., Ltd
- 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
- QMS/QSD;; 國產
- Registration Date
- Oct 31, 2019
- Expiry Date
- Oct 31, 2029
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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.