Taiwan FDA registration aa38eaa6f71b00c8c77fef9def8534ae
"Siemens" 800 series lotion and metabolic analysis corrector
TW: “西門子”800系列 洗液暨代謝分析校正品
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered Aug 25, 2010 – Aug 25, 2020CancelledRegistration details
- Analysis ID
- aa38eaa6f71b00c8c77fef9def8534ae
- Customs Code
- DHA00602140707
Company information
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- It is used in the "Ximenzi" 800 series blood gas analysis series as a cleaning test line and providing a two-point proxy correction.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Aug 25, 2010
- Expiry Date
- Aug 25, 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 lotion and metabolic analysis corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa38eaa6f71b00c8c77fef9def8534ae and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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