Taiwan FDA registration f1887b0034f0ded0420db626973c112e
"Pushen" Helicobacter pylori IgM enzyme immunoassay group (unsterilized)
TW: "普生" 幽門螺旋桿菌IgM酵素免疫分析組 (未滅菌)
Taiwan·Risk Class 1·GENERAL BIOLOGICALS CORP.·Registered Jul 31, 2014 – Jul 31, 2024ExpiredRegistration details
- Analysis ID
- f1887b0034f0ded0420db626973c112e
Company information
- Manufacturer
- GENERAL BIOLOGICALS CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
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
- Domestic
Dates and status
- Registration Date
- Jul 31, 2014
- Expiry Date
- Jul 31, 2024
About this record
Access comprehensive regulatory information for "Pushen" Helicobacter pylori IgM enzyme immunoassay group (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f1887b0034f0ded0420db626973c112e and manufactured by GENERAL BIOLOGICALS CORP.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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