Taiwan FDA registration 5a0631a110e20fba3b664c6da7b034b0
SD BIOSENSOR STANDARD F RSV Ag FIA (Non-Sterile)
TW: “速得百森” 呼吸道融合細胞病毒血清試劑(未滅菌)
Taiwan·Risk Class 1·MD·SD BIOSENSOR, Inc.·Registered Jan 21, 2019 – Jan 21, 2024ExpiredRegistration details
- Analysis ID
- 5a0631a110e20fba3b664c6da7b034b0
- License Form
- Ministry of Health Medical Device Import No. 020047
- Customs Code
- DHA09402004701
Company information
- Manufacturer
- SD BIOSENSOR, Inc.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- CREATIVE LIFE SCIENCE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Respiratory Fusion Cell Virus Serological Reagent (C.3480)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3480 Respiratory Fusion Cell Virus Serological Reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 21, 2019
- Expiry Date
- Jan 21, 2024
About this record
Access comprehensive regulatory information for SD BIOSENSOR STANDARD F RSV Ag FIA (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 5a0631a110e20fba3b664c6da7b034b0 and manufactured by SD BIOSENSOR, Inc.. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE CO., LTD..
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