Taiwan FDA registration b198b5a0155a0c480b3d139d7621aa91
Wonderford Influenza A/B Virus Rapid Test Reagent (Unsterilized)
TW: 萬德福A/B型流感病毒快速檢測試劑(未滅菌)
Taiwan·Risk Class 1·WONDFO BIOTECH CO., LTD·Registered Sep 30, 2009 – Sep 30, 2024ExpiredRegistration details
- Analysis ID
- b198b5a0155a0c480b3d139d7621aa91
- Customs Code
- DHA04600080308
Company information
- Manufacturer
- WONDFO BIOTECH CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
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
- Chinese goods;; input
Dates and status
- Registration Date
- Sep 30, 2009
- Expiry Date
- Sep 30, 2024
About this record
Access comprehensive regulatory information for Wonderford Influenza A/B 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 b198b5a0155a0c480b3d139d7621aa91 and manufactured by WONDFO BIOTECH CO., LTD. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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