Taiwan FDA registration d38507efe8535802700f3dbc944a4329
"Siemens" automatic urine analyzer correction solution group
TW: “西門子”全自動尿液分析儀 校正液組
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered Sep 16, 2010 – Sep 16, 2025ExpiredRegistration details
- Analysis ID
- d38507efe8535802700f3dbc944a4329
- Customs Code
- DHA00602154101
Company information
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- THIS CORRECTION SOLUTION IS USED IN CONJUNCTION WITH CLINITEK TLAS REAGENTS TO CORRECT THE FULLY AUTOMATED URINE ANALYZER CLINITEK ATLAS.
- 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 16, 2010
- Expiry Date
- Sep 16, 2025
About this record
Access comprehensive regulatory information for "Siemens" automatic urine analyzer correction solution group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d38507efe8535802700f3dbc944a4329 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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