Dual-function inspection system for automatic film withdrawal (unsterilized)
Taiwan·Risk Class 1·Qinli Biotechnology Co., Ltd. New North Plant·Registered Oct 12, 2022 – Oct 12, 2027Active- Analysis ID
- 595a2f6b3ee92b67d8d8c27ab0858ed5
- Manufacturer
- Qinli Biotechnology Co., Ltd. New North Plant
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENERAL LIFE BIOTECHNOLOGY CO., LTD.
- Intended Use
- Limited to the classification and grading management of medical devices, "cholesterol (total) test system (A.1175), uric acid test system (A.1775)", "quality control materials (analytical and non-analytical) (A.1660)", "manual instruments for general surgery (I.4800)" first grade identification range.
- 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
- 國產;; QMS/QSD
- Registration Date
- Oct 12, 2022
- Expiry Date
- Oct 12, 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 595a2f6b3ee92b67d8d8c27ab0858ed5 and manufactured by Qinli Biotechnology Co., Ltd. New North Plant. The authorized representative in Taiwan is GENERAL LIFE BIOTECHNOLOGY CO., LTD..
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