Taiwan FDA registration 27528149da3b82d4a5d3a6634acbecd3
IMAGEN Influenza Virus A and B (Non-Sterile)
TW: "賽默飛世爾科技" A和B型流感病毒抗原螢光檢驗試劑套組(未滅菌)
Taiwan·Risk Class 1·MD·OXOID LIMITED·Registered Aug 01, 2019 – Aug 01, 2024ExpiredRegistration details
- Analysis ID
- 27528149da3b82d4a5d3a6634acbecd3
- License Form
- Ministry of Health Medical Device Import No. 020710
- Customs Code
- DHA09402071003
Company information
- Manufacturer
- OXOID LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3330 Influenza virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 01, 2019
- Expiry Date
- Aug 01, 2024
About this record
Access comprehensive regulatory information for IMAGEN Influenza Virus A and B (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 27528149da3b82d4a5d3a6634acbecd3 and manufactured by OXOID LIMITED. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..
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