Taiwan FDA registration 5688c3a28637a3322e9fb7ed2c4a711f
Beckman Coulter Access Sensitive Estradiol Calibrators
TW: 貝克曼庫爾特亞瑟斯敏感雌二醇校正液
Taiwan·Risk Class 2·MD·IMMUNOTECH SAS, A BECKMAN COULTER COMPANY·Registered Nov 16, 2018 – Nov 16, 2023ExpiredRegistration details
- Analysis ID
- 5688c3a28637a3322e9fb7ed2c4a711f
- License Form
- Ministry of Health Medical Device Import No. 031787
- Customs Code
- DHA05603178703
Company information
- Manufacturer
- IMMUNOTECH SAS, A BECKMAN COULTER COMPANY
- Manufacturer Country
- France
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- This product is used to correct the Access Sensitive Estradiol analysis, which is used with the Access Immunoassay System to quantitatively detect estradiol concentrations in human serum and plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1150 calibrate
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 16, 2018
- Expiry Date
- Nov 16, 2023
About this record
Access comprehensive regulatory information for Beckman Coulter Access Sensitive Estradiol Calibrators in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5688c3a28637a3322e9fb7ed2c4a711f and manufactured by IMMUNOTECH SAS, A BECKMAN COULTER COMPANY. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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