Taiwan FDA registration ca944a36a3caf32bd043760c5f228521
"Microacytic" Pylori antigen test reagent (unsterilized)
TW: "微栩" 幽門桿菌抗原檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·ZHONGSHAN MAI SHENG MEDICAL TECHNOLOGY CO., LTD·Registered Aug 13, 2020 – Aug 13, 2025ExpiredRegistration details
- Analysis ID
- ca944a36a3caf32bd043760c5f228521
- Customs Code
- DHA09600429005
Company information
- Manufacturer
- ZHONGSHAN MAI SHENG MEDICAL TECHNOLOGY CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- WISH IN COMPANY LIMITED
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
- Aug 13, 2020
- Expiry Date
- Aug 13, 2025
About this record
Access comprehensive regulatory information for "Microacytic" Pylori antigen 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 ca944a36a3caf32bd043760c5f228521 and manufactured by ZHONGSHAN MAI SHENG MEDICAL TECHNOLOGY CO., LTD. The authorized representative in Taiwan is WISH IN COMPANY LIMITED.
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