Taiwan FDA registration c5d11f8a8c6c8d1ee336faf895af49a4
"Microgen" Salmonella Antisera Reagent（Non-Sterile）
TW: "邁克奇" 沙門氏菌抗血清試劑（未滅菌）
Taiwan·Risk Class 1·MD·MICROGEN BIOPRODUCTS LTD·Registered Apr 26, 2019 – Apr 26, 2024ExpiredRegistration details
- Analysis ID
- c5d11f8a8c6c8d1ee336faf895af49a4
- License Form
- Ministry of Health Medical Device Import No. 020378
- Customs Code
- DHA09402037808
Company information
- Manufacturer
- MICROGEN BIOPRODUCTS LTD
- Manufacturer Country
- United Kingdom
- Authorized Representative
- GLOWAY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Salmonella Serological Reagent (C.3550)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3550 Salmonella serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 26, 2019
- Expiry Date
- Apr 26, 2024
About this record
Access comprehensive regulatory information for "Microgen" Salmonella Antisera Reagent（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 c5d11f8a8c6c8d1ee336faf895af49a4 and manufactured by MICROGEN BIOPRODUCTS LTD. The authorized representative in Taiwan is GLOWAY CO., LTD..
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