Taiwan FDA registration fc0a1b55aa74f3ca966a66dddd8282dd
"ACRO" RotaVirus test kit (Non-sterile)
TW: "愛可羅" 輪狀病毒檢驗試劑組(未滅菌)
Taiwan·Risk Class 1·MD·ACRO BIOTECH. INC.·Registered Apr 29, 2019 – Apr 29, 2024ExpiredRegistration details
- Analysis ID
- fc0a1b55aa74f3ca966a66dddd8282dd
- License Form
- Ministry of Health Medical Device Import No. 020382
- Customs Code
- DHA09402038202
Company information
- Manufacturer
- ACRO BIOTECH. INC.
- Manufacturer Country
- United States
- Authorized Representative
- APPLIED BIOTECH ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Polio Virus Serological Reagent (C.3405)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3405 Polio virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 29, 2019
- Expiry Date
- Apr 29, 2024
About this record
Access comprehensive regulatory information for "ACRO" RotaVirus 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 fc0a1b55aa74f3ca966a66dddd8282dd and manufactured by ACRO BIOTECH. INC.. The authorized representative in Taiwan is APPLIED BIOTECH ENTERPRISE CO., LTD..
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