sTfR
Basic Information
- Primary DI
- 16438153000706
- Basic UDI-DI Code
- 6438153BU00124BL
- Reference
- 981945
- Device Types
- None provided
- Regulation
- Eu Ivdr
- Classification
- Eu Ivd Class B
- Status
- On The Market
- Manufacturer
- Thermo Fisher Scientific Oy
Additional Description
INTENDED PURPOSE / INTENDED USE For in vitro diagnostic use in the quantitative determination of the soluble transferrin receptor (sTfR) concentration in human serum and plasma with the automated procedures of Thermo Scientificโข Indikoโข and Konelabโข analyzers. The sTfR test is indicated to be used in conjunction with clinical evaluation for aid to differential diagnosis of iron deficiency anemia (IDA) and anemia of chronic disorders (ACD), in patients. Furthermore, the sTfR test is indicated to be used in conjunction with clinical evaluation for aid to diagnosis of hemolytic anemia, polycythemia and thalassemia without iron deficiency, in patients. The sTfR test is also indicated to be used in conjunction with clinical evaluation for aid to diagnosis of functional iron deficiency (FID) and monitoring of sTfR values during erythropoietin (EPO) therapy for preventing FID caused by rapid or impaired mobilization of iron stores, in patients.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0102070104 | SOLUBLE TRANSFERRIN RECEPTOR |
Available In Countries
Similar Devices
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