Taiwan FDA registration c95786a496227cbc8aa78180bde11bef
"Core generation" influenza virus reagent (unsterilized)
TW: "芯世代"流行性感冒病毒試劑(未滅菌)
Taiwan·Risk Class 1·Xintang Enterprise Co., Ltd. Taichung Factory·Registered Oct 24, 2016 – Oct 24, 2021CancelledRegistration details
- Analysis ID
- c95786a496227cbc8aa78180bde11bef
Company information
- Manufacturer
- Xintang Enterprise Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENPRONEX INC.
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
- Product Type (Level 2)
- C.3330 流感病毒血清試劑
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Oct 24, 2016
- Expiry Date
- Oct 24, 2021
- Cancellation Date
- May 12, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Core generation" influenza virus reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c95786a496227cbc8aa78180bde11bef and manufactured by Xintang Enterprise Co., Ltd. Taichung Factory. The authorized representative in Taiwan is GENPRONEX INC..
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