"Ruibang Biomedical" Lemp fluorescence analyzer (unsterilized)
Taiwan·Risk Class 1·RESPONSE BIOMEDICAL CORPORATION·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- 56539d6b6c7d768d114a0beaee84a6e5
- Customs Code
- DHA08401535802
- Manufacturer
- RESPONSE BIOMEDICAL CORPORATION
- Manufacturer Country
- Canada
- Authorized Representative
- RECHI CO., LTD.
- Intended Use
- Limited to the classification and grading management measures of medical equipment "fluorescence instrument for clinical use (A.2560)" the first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2560 Fluorometer for clinical use
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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Access comprehensive regulatory information for "Ruibang Biomedical" Lemp fluorescence analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 56539d6b6c7d768d114a0beaee84a6e5 and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..
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