Taiwan FDA registration f491e219cf71601eeb5c96d8d2cc87a2
"Wanfu" Helicobacter pylori test kit (serum/plasma) (unsterilized)
TW: “萬福” 幽門螺旋桿菌檢測試劑盒(血清/血漿) (未滅菌)
Taiwan·Risk Class 1·GUANGZHOU WONDFO BIOTECH CO., LTD.·Registered Jan 20, 2020 – Jan 20, 2025ExpiredRegistration details
- Analysis ID
- f491e219cf71601eeb5c96d8d2cc87a2
- Customs Code
- DHA09600407807
Company information
- Manufacturer
- GUANGZHOU WONDFO BIOTECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- HUNGAN MEDICAL CO.
Product details
- Intended Use
- Limited to the classification and grading management of medical devices, the first level identification range of "Helicobacter serum reagent (C.0003)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.0003 螺旋桿菌屬血清試劑
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jan 20, 2020
- Expiry Date
- Jan 20, 2025
About this record
Access comprehensive regulatory information for "Wanfu" Helicobacter pylori test kit (serum/plasma) (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f491e219cf71601eeb5c96d8d2cc87a2 and manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD.. The authorized representative in Taiwan is HUNGAN MEDICAL CO..
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