Taiwan FDA registration a995ec51403524fc2931c92444750c4e
"Lingyue" respiratory fusion cell virus rapid test reagent (unsterilized)
TW: “凌越”呼吸道融合細胞病毒快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·Lingyue Biomedical Co., Ltd. Taipei Factory·Registered Aug 26, 2013 – Aug 26, 2018CancelledRegistration details
- Analysis ID
- a995ec51403524fc2931c92444750c4e
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 "Respiratory Fusion Cell Virus Serological Reagent (C.3480)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3480 呼吸道融合細胞病毒血清試劑
- 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" respiratory fusion cell 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 a995ec51403524fc2931c92444750c4e 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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