Taiwan FDA registration 4b38d35ed4bf49e2a7e8cff72ac4cb23
"Siemens" 800 series metabolic analysis correctors
TW: “西門子”800系列 代謝分析校正品
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered Sep 24, 2010 – Sep 24, 2020CancelledRegistration details
- Analysis ID
- 4b38d35ed4bf49e2a7e8cff72ac4cb23
- Customs Code
- DHA00602155203
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, it provides single-point correction and slope point two-point substitution correction.
- 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 24, 2010
- Expiry Date
- Sep 24, 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 metabolic analysis correctors in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b38d35ed4bf49e2a7e8cff72ac4cb23 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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