Taiwan FDA registration 8fe0e19c3e46cc11aa8c0a4c00446c97
"Thermo Fisher Scientific" Rotavirus Antigen Rapid Test (Non-sterile)
TW: "賽默飛世爾科技" 輪狀病毒抗原快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·REMEL INC.·Registered Nov 14, 2016 – Nov 14, 2021ExpiredRegistration details
- Analysis ID
- 8fe0e19c3e46cc11aa8c0a4c00446c97
- License Form
- Ministry of Health Medical Device Import No. 017174
- Customs Code
- DHA09401717408
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 "Polio Virus Serological Reagent (C.3405)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3405 Polio virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 14, 2016
- Expiry Date
- Nov 14, 2021
About this record
Access comprehensive regulatory information for "Thermo Fisher Scientific" Rotavirus Antigen Rapid Test (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 8fe0e19c3e46cc11aa8c0a4c00446c97 and manufactured by REMEL INC.. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..
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