Taiwan FDA registration 75c996a85493190ecee764f2c7078040
"Siemens" lithium testing reagent
TW: “西門子” 鋰檢驗試劑
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Mar 11, 2022 – Mar 11, 2027ActiveRegistration details
- Analysis ID
- 75c996a85493190ecee764f2c7078040
- Customs Code
- DHA05603522800
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- This product is used with Atellica CH Analyzer to quantitatively detect lithium in human serum and plasma (heparin sodium or EDTA potassium salt).
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3560 Lithium Test System
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 11, 2022
- Expiry Date
- Mar 11, 2027
About this record
Access comprehensive regulatory information for "Siemens" lithium testing reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 75c996a85493190ecee764f2c7078040 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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