Taiwan FDA registration a86b3d98631e94851afa54bce3f18d82
"IF" Rapid Helicobacter Test (non-sterile)
TW: "瑩芳"幽門曲狀桿菌尿素酶快速測試組(未滅菌)
Taiwan·Risk Class 1·MD·Yingfang Co., Ltd. Taichung Factory·Registered Jun 24, 2019 – Jun 24, 2024ExpiredRegistration details
- Analysis ID
- a86b3d98631e94851afa54bce3f18d82
- License Form
- Ministry of Health Medical Device Manufacturing No. 007818
Company information
- Manufacturer
- Yingfang Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C0003 Helicobacter serological reagent
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jun 24, 2019
- Expiry Date
- Jun 24, 2024
About this record
Access comprehensive regulatory information for "IF" Rapid Helicobacter Test (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a86b3d98631e94851afa54bce3f18d82 and manufactured by Yingfang Co., Ltd. Taichung Factory. The authorized representative in Taiwan is IN FUNG CO., LTD..
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