Taiwan FDA registration 42c7aa90ca47644773e20923c7015849
“GenBody” Influenza A＆B Ag (Non-Sterile)
TW: “基因巴帝”流感病毒A＆B抗原快速檢驗試劑(未滅菌)
Taiwan·Risk Class 1·MD·GENBODY INC.·Registered Nov 19, 2018 – Nov 19, 2023ExpiredRegistration details
- Analysis ID
- 42c7aa90ca47644773e20923c7015849
- License Form
- Ministry of Health Medical Device Import No. 019830
- Customs Code
- DHA09401983000
Company information
- Manufacturer
- GENBODY INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EVERMEDICAL COMPANY LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3330 Influenza virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 19, 2018
- Expiry Date
- Nov 19, 2023
About this record
Access comprehensive regulatory information for “GenBody” Influenza A＆B Ag (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 42c7aa90ca47644773e20923c7015849 and manufactured by GENBODY INC.. The authorized representative in Taiwan is EVERMEDICAL COMPANY LTD..
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