Taiwan FDA registration 63a21e1acae34c7bcdcd95c826ce149a
"Siemens" wide range of C-reactive protein correctors
TW: “西門子”寬範圍 C 反應蛋白校正品
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Sep 19, 2008 – Sep 19, 2028ActiveRegistration details
- Analysis ID
- 63a21e1acae34c7bcdcd95c826ce149a
- Customs Code
- DHA00601944204
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- In vitro diagnostic test for the detection of a wide range of C-reactive protein (wrCRP) by the ADVIA biochemical analysis system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Sep 19, 2008
- Expiry Date
- Sep 19, 2028
About this record
Access comprehensive regulatory information for "Siemens" wide range of C-reactive protein correctors in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 63a21e1acae34c7bcdcd95c826ce149a and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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