Taiwan FDA registration c5f65dc7098ef68ecf37ae0fa58aef57
"Siemens" 800 series 6.838 corrector
TW: “西門子”800系列6.838校正品
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered Oct 01, 2010 – Oct 01, 2020CancelledRegistration details
- Analysis ID
- c5f65dc7098ef68ecf37ae0fa58aef57
- Customs Code
- DHA00602155700
Company information
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Used in the "Ximenzi" 800 series blood gas analysis series, the slope point is provided as the anometer value and electrolyte correction for the anolyte.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Oct 01, 2010
- Expiry Date
- Oct 01, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Siemens" 800 series 6.838 corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5f65dc7098ef68ecf37ae0fa58aef57 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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