Taiwan FDA registration 5c8bd293072403594b6358a9d88d58ba
Siemens electrolyte buffer
TW: 西門子電解質緩衝液
Taiwan·Risk Class 2·JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Mar 17, 2017 – Mar 17, 2027ActiveRegistration details
- Analysis ID
- 5c8bd293072403594b6358a9d88d58ba
- Customs Code
- DHA05602951504
Company information
- Manufacturer
- JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.
- Manufacturer Country
- United States;;Japan
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Quantitatively detect the concentration of electrolytes in human serum, plasma and urine with ADVIA chemical XPT system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1170 氯化物試驗系統;; A.1665 鈉試驗系統;; A.1600 鉀試驗系統
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Mar 17, 2017
- Expiry Date
- Mar 17, 2027
About this record
Access comprehensive regulatory information for Siemens electrolyte buffer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5c8bd293072403594b6358a9d88d58ba and manufactured by JEOL LTD.;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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