Thermo Fisher Scientific Respiratory Fusion Viral Antigen Fluorescence Test Kit (Unsterilized)
Taiwan·Risk Class 1·OXOID LIMITED;; Remel Europe Limited·Registered Jul 10, 2024 – Jul 10, 2029Active- Analysis ID
- 50662dbb2c1fbc6342e97972d2d54db1
- Customs Code
- DHA09402353401
- Manufacturer
- OXOID LIMITED;; Remel Europe Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.
- Intended Use
- It is limited to the first level of identification of the "Respiratory Fusion Cell Virus Serum Reagent (C.3480)" of the Classification and Grading Management Measures for Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3480 呼吸道融合細胞病毒血清試劑
- Import Information
- Input;; QMS/QSD
- Registration Date
- Jul 10, 2024
- Expiry Date
- Jul 10, 2029
Access comprehensive regulatory information for Thermo Fisher Scientific Respiratory Fusion Viral Antigen Fluorescence Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 50662dbb2c1fbc6342e97972d2d54db1 and manufactured by OXOID LIMITED;; Remel Europe Limited. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..
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