Taiwan FDA registration a0c32a44cc296916c20ce9e5861487d6
"Siemens" C-reactive protein corrector
TW: “西門子”C 反應蛋白校正品
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Aug 22, 2008 – Aug 22, 2013CancelledRegistration details
- Analysis ID
- a0c32a44cc296916c20ce9e5861487d6
- Customs Code
- DHA00601942708
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS LIMITED
Product details
- Intended Use
- In vitro diagnostic test for the detection of C-reactive protein by the calibration 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
- Aug 22, 2008
- Expiry Date
- Aug 22, 2013
- Cancellation Date
- Aug 10, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Siemens" C-reactive protein corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0c32a44cc296916c20ce9e5861487d6 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS LIMITED.
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