Taiwan FDA registration 0077b11478227e116aa1289ccfe1e61b
"Siemens" LDL cholesterol corrector
TW: “西門子” 低密度脂蛋白膽固醇校正品
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Mar 17, 2022 – Mar 17, 2027ActiveRegistration details
- Analysis ID
- 0077b11478227e116aa1289ccfe1e61b
- Customs Code
- DHA05603522902
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- For in vitro diagnostic use, in combination with the Atellica Chemical Analyzer for the calibration of the Atellica CH LDL Cholesterol (LDLC) test.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 17, 2022
- Expiry Date
- Mar 17, 2027
About this record
Access comprehensive regulatory information for "Siemens" LDL cholesterol corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0077b11478227e116aa1289ccfe1e61b and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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