Taiwan FDA registration b09c5d0786ebcc3b1e6170f86253ab88
Ningli A+B Influenza Virus Rapid Test Set (Unsterilized)
TW: 寧立 A+B 型流行性感冒病毒快速檢驗試劑組(未滅菌)
Taiwan·Risk Class 1·LINEAR CHEMICALS S.L.·Registered Oct 12, 2009 – Oct 12, 2014CancelledRegistration details
- Analysis ID
- b09c5d0786ebcc3b1e6170f86253ab88
- Customs Code
- DHA04400820206
Company information
- Manufacturer
- LINEAR CHEMICALS S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- LIKWANG INSTRUMENTS 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
- Product Type (Level 2)
- C.3330 流感病毒血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Oct 12, 2009
- Expiry Date
- Oct 12, 2014
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Ningli A+B Influenza Virus Rapid Test Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b09c5d0786ebcc3b1e6170f86253ab88 and manufactured by LINEAR CHEMICALS S.L.. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..
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