"Ruibang Biomedical" Lemp fluorescence analyzer (unsterilized)
Taiwan·Risk Class 1·RESPONSE BIOMEDICAL CORPORATION·Registered Jun 17, 2015 – Jun 17, 2025Cancelled- Analysis ID
- 52cd3eea9032f0e4ac7c4873ae42e556
- Customs Code
- DHA09401535808
- Manufacturer
- RESPONSE BIOMEDICAL CORPORATION
- Manufacturer Country
- Canada
- Authorized Representative
- RECHI CO., LTD.
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Fluorescence Instrument for Clinical Use (A.2560)".
- 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
- Jun 17, 2015
- Expiry Date
- Jun 17, 2025
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 52cd3eea9032f0e4ac7c4873ae42e556 and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..
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