Taiwan FDA registration 163b5661f32c0c186915aeab60e0e200
"MIZUHO" Adenovirus test kit (Non-sterile)
TW: "美日和"腺病毒檢驗試劑組(未滅菌)
Taiwan·Risk Class 1·MD·MIZUHO MEDY CO., LTD.·Registered Feb 05, 2018 – Feb 05, 2023ExpiredRegistration details
- Analysis ID
- 163b5661f32c0c186915aeab60e0e200
- License Form
- Ministry of Health Medical Device Import No. 018791
- Customs Code
- DHA09401879101
Company information
- Manufacturer
- MIZUHO MEDY CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- LINKSEAS TRADING CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3020 adenovirus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 05, 2018
- Expiry Date
- Feb 05, 2023
About this record
Access comprehensive regulatory information for "MIZUHO" Adenovirus test kit (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 163b5661f32c0c186915aeab60e0e200 and manufactured by MIZUHO MEDY CO., LTD.. The authorized representative in Taiwan is LINKSEAS TRADING CO., LTD..
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