Taiwan FDA registration 8b664742d6370bef0e820da4c97b261a
"Microgen" Staph Rapid Test (Non-Sterile)
TW: "邁克奇"金黃色葡萄球菌乳膠凝集測定試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·MICROGEN BIOPRODUCTS LTD·Registered Jul 13, 2018 – Jul 13, 2023ExpiredRegistration details
- Analysis ID
- 8b664742d6370bef0e820da4c97b261a
- License Form
- Ministry of Health Medical Device Import No. 019305
- Customs Code
- DHA09401930507
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 "Staphylococcus aureus serum reagent (C.3700)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3700 Staphylococcus aureus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 13, 2018
- Expiry Date
- Jul 13, 2023
About this record
Access comprehensive regulatory information for "Microgen" Staph Rapid 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 8b664742d6370bef0e820da4c97b261a and manufactured by MICROGEN BIOPRODUCTS LTD. The authorized representative in Taiwan is GLOWAY CO., LTD..
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