Taiwan FDA registration e4e8237b1c9a21feee6a03d47f8208c1
"Siemens" creatine stimulation per reagent set
TW: “西門子”肌酸激每試劑組
Taiwan·Risk Class 2·RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jan 24, 2008 – Jan 24, 2023ExpiredRegistration details
- Analysis ID
- e4e8237b1c9a21feee6a03d47f8208c1
- Customs Code
- DHA00601894308
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Quantitatively determine the activity of creatine kines in human serum and plasma on the ADVIA automated chemical analysis system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1215 Creatine phosphokinase/creatine kinase or isoenzyme testing system
- Import Information
- import
Dates and status
- Registration Date
- Jan 24, 2008
- Expiry Date
- Jan 24, 2023
About this record
Access comprehensive regulatory information for "Siemens" creatine stimulation per reagent set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4e8237b1c9a21feee6a03d47f8208c1 and manufactured by RANDOX LABORATORIES LIMITED;; SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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