Taiwan FDA registration 3f49279c01150054b056e1c1d0e5409e
Rapid Test Reagent for Influenza Virus A and B (Unsterilized)
TW: 醫試美流行性感冒病毒A型及B型快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·Kaiwu Technology Co., Ltd. Nanke Factory·Registered Jan 27, 2014 – Jan 27, 2024ExpiredRegistration details
- Analysis ID
- 3f49279c01150054b056e1c1d0e5409e
Company information
- Manufacturer
- Kaiwu Technology Co., Ltd. Nanke Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Kaiwu Technology Co., Ltd. Nanke Factory
Product details
- Intended Use
- It is limited to the first-level identification scope of influenza virus serum reagent (C.3330) in the classification and grading management measures for medical devices.
- 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
- Jan 27, 2014
- Expiry Date
- Jan 27, 2024
About this record
Access comprehensive regulatory information for Rapid Test Reagent for Influenza Virus A and B (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3f49279c01150054b056e1c1d0e5409e and manufactured by Kaiwu Technology Co., Ltd. Nanke Factory. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Nanke Factory.
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