Taiwan FDA registration 7dca613e36653bdbe5cae55642bee14a
"Siemens" electrolyte urine standard
TW: “西門子”電解質尿液標準液
Taiwan·Risk Class 2·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Mar 02, 2009 – Mar 02, 2029ActiveRegistration details
- Analysis ID
- 7dca613e36653bdbe5cae55642bee14a
- Customs Code
- DHA00601995800
Company information
- Manufacturer
- JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States;;Japan
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- It is used in the Siemens ADVIA chemical system to quantitatively measure the concentration of sodium, potassium, and chloride ions in human urine.
- 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
- Mar 02, 2009
- Expiry Date
- Mar 02, 2029
About this record
Access comprehensive regulatory information for "Siemens" electrolyte urine standard in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7dca613e36653bdbe5cae55642bee14a and manufactured by JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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