Taiwan FDA registration 0f77d9a3b6ca7fbaf0977251ea4b836f
"Siemens" electrolyte reference solution
TW: “西門子”電解質參考液
Taiwan·Risk Class 2·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Apr 01, 2009 – Apr 01, 2024ExpiredRegistration details
- Analysis ID
- 0f77d9a3b6ca7fbaf0977251ea4b836f
- Customs Code
- DHA00601997704
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 electrolytes in human serum, plasma and urine.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1665 Sodium Test System
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Apr 01, 2009
- Expiry Date
- Apr 01, 2024
About this record
Access comprehensive regulatory information for "Siemens" electrolyte reference solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f77d9a3b6ca7fbaf0977251ea4b836f and manufactured by JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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