Beckman Coulter Arthurs Sex Hormone-Binding Globulin Correction Solution and Quality Control Solution
Taiwan·Risk Class 2·IMMUNOTECH SAS, A BECKMAN COULTER COMPANY·Registered Dec 21, 2018 – Dec 21, 2028Active- Analysis ID
- feddbee51841aca93d57264a712922cb
- Customs Code
- DHA05603197902
- Manufacturer
- IMMUNOTECH SAS, A BECKMAN COULTER COMPANY
- Manufacturer Country
- France
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
- Intended Use
- Calibration Solution: This product is used to correct the Access SHBG assay, which uses the Access Immunoassay System to quantitatively measure the concentration of human serum and plasma neuterine-binding globulin. Quality control fluid: This product is used for access SHBG testing quality control.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 calibration;; A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- import
- Registration Date
- Dec 21, 2018
- Expiry Date
- Dec 21, 2028
Access comprehensive regulatory information for Beckman Coulter Arthurs Sex Hormone-Binding Globulin Correction Solution and Quality Control Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number feddbee51841aca93d57264a712922cb 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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