Taiwan FDA registration 124800feb9706006771f82385e71431f
"Siemens" ISE electrolyte serum standard
TW: “西門子”ISE 電解質血清標準液
Taiwan·Risk Class 2·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Nov 24, 2008 – Nov 24, 2028ActiveRegistration details
- Analysis ID
- 124800feb9706006771f82385e71431f
- Customs Code
- DHA00601959809
Company information
- Manufacturer
- JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States;;Japan
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Quantitatively measure the concentration of sodium, potassium, and chloride ions in human serum and plasma.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Nov 24, 2008
- Expiry Date
- Nov 24, 2028
About this record
Access comprehensive regulatory information for "Siemens" ISE electrolyte serum standard in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 124800feb9706006771f82385e71431f and manufactured by JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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