Taiwan FDA registration f963ffa397f1068a58d78eaafd91df11
"Siemens" urea nitrogen reagent group
TW: “西門子”尿素氮試劑組
Taiwan·Risk Class 2·RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jan 24, 2008 – Jan 24, 2028ActiveRegistration details
- Analysis ID
- f963ffa397f1068a58d78eaafd91df11
- Customs Code
- DHA00601894002
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Quantitatively determine urea nitrogen in human serum, plasma, and urine on the ADVIA automated chemical analysis system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1770 尿素氮試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Jan 24, 2008
- Expiry Date
- Jan 24, 2028
About this record
Access comprehensive regulatory information for "Siemens" urea nitrogen reagent group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f963ffa397f1068a58d78eaafd91df11 and manufactured by RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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