Taiwan FDA registration 47cfd835251eae20756802e852a494f5
"Lingyue" A/B influenza virus rapid test reagent (unsterilized)
TW: “凌越”A/B型流行性感冒病毒快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·Lingyue Biomedical Co., Ltd. Taipei Factory·Registered Aug 26, 2013 – Aug 26, 2018CancelledRegistration details
- Analysis ID
- 47cfd835251eae20756802e852a494f5
Company information
- Manufacturer
- Lingyue Biomedical Co., Ltd. Taipei Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Lingyue Biomedical Co., Ltd. Taipei Factory
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
Dates and status
- Registration Date
- Aug 26, 2013
- Expiry Date
- Aug 26, 2018
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Lingyue" A/B influenza virus rapid test 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 47cfd835251eae20756802e852a494f5 and manufactured by Lingyue Biomedical Co., Ltd. Taipei Factory. The authorized representative in Taiwan is Lingyue Biomedical Co., Ltd. Taipei Factory.
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