Dual-function inspection system for automatic film withdrawal (unsterilized)
Taiwan·Risk Class 1·Qinli Biotechnology Co., Ltd. new tree factory·Registered May 25, 2017 – May 25, 2027Active- Analysis ID
- a4b2e767ebebd5f5399d4fed4c854a54
- Manufacturer
- Qinli Biotechnology Co., Ltd. new tree factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENERAL LIFE BIOTECHNOLOGY CO., LTD.
- Intended Use
- It is limited to the first level of the classification and grading management measures for medical devices, "Quality Control Materials (Analytical and Non-Analytical) (A.1660)", "Uric Acid Test System (A.1775)", "Manual Instruments for General Surgery (I.4800)", and "Cholesterol (Total) Test System (A.1175)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1775 Uric acid test system;; A.1660 Grade Material (Analysis Material Non-Analysis);; A.1175 膽固醇(總量)試驗系統
- Import Information
- QMS/QSD;; 國產
- Registration Date
- May 25, 2017
- Expiry Date
- May 25, 2027
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Access comprehensive regulatory information for Dual-function inspection system for automatic film withdrawal (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a4b2e767ebebd5f5399d4fed4c854a54 and manufactured by Qinli Biotechnology Co., Ltd. new tree factory. The authorized representative in Taiwan is GENERAL LIFE BIOTECHNOLOGY CO., LTD..
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