Taiwan FDA registration fc730c962bef3a3cb13dda68f8441853
LIAISON CMV IgM II
TW: 禮亞尚巨細胞病毒IgM檢測試劑 第二代
Taiwan·Risk Class 2·MD·DIASORIN ITALIA S.P.A.·Registered Jul 22, 2014 – Jul 22, 2024ExpiredRegistration details
- Analysis ID
- fc730c962bef3a3cb13dda68f8441853
- License Form
- Ministry of Health Medical Device Import No. 026277
- Customs Code
- DHA05602627702
Company information
- Manufacturer
- DIASORIN ITALIA S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- This product uses chemical cold light particle immunoassay (CLIA) method to semi-quantify cytomegalovirus IgM antibodies in human serum and plasma. It must be used with a Liashang analyzer for detection and analysis.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3175 CMV serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 22, 2014
- Expiry Date
- Jul 22, 2024
About this record
Access comprehensive regulatory information for LIAISON CMV IgM II in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc730c962bef3a3cb13dda68f8441853 and manufactured by DIASORIN ITALIA S.P.A.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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