Taiwan FDA registration d9e1886b6b97ec4670896e1f0237d1cd
"Thermo Fisher Scientific" Respiratory syncytial virus serological reagents (Non-Sterile)
TW: "賽默飛世爾科技" 呼吸道融合細胞病毒血清試劑 (未滅菌)
Taiwan·Risk Class 1·MD·REMEL INC.·Registered Dec 02, 2015 – Dec 02, 2025ExpiredRegistration details
- Analysis ID
- d9e1886b6b97ec4670896e1f0237d1cd
- License Form
- Ministry of Health Medical Device Import No. 015921
- Customs Code
- DHA09401592109
Company information
- Manufacturer
- REMEL INC.
- Manufacturer Country
- United States
- 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 "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
- Dec 02, 2015
- Expiry Date
- Dec 02, 2025
About this record
Access comprehensive regulatory information for "Thermo Fisher Scientific" Respiratory syncytial virus serological reagents (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 d9e1886b6b97ec4670896e1f0237d1cd and manufactured by REMEL INC.. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..
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