UIBC Calibrator: Package Size Intended Use
UIBC Calibrator: Package Size Intended Use
UIBC Calibrator: Package Size Intended Use
Package size
1×1 level×1 mL
Intended use
UIBC Calibrator is used for the calibration of quantitative determination of
Unsaturated Iron Binding Capacity (UIBC) on Mindray BS measurement
system.
Summary
UIBC Calibrator contains ammonium iron(II) sulfate hexahydrate analyte.
By calibrating the selected analytes, Mindray BS-series chemistry analyzers
can generate valid calibration factors, and then calculate the activities of
each sample automatically after analysis. Mindray BS measurement system
is composed of Mindray BS-series chemistry analyzers, Mindray reagent kits,
calibrators and control materials.
Components
UIBC Calibrator is a liquid calibrator based on ammonium iron(II) sulfate
hexahydrate. The concentrations of the calibrator components are
lot-specific.
Warnings and Precautions
1.For in vitro diagnostic use only.
2.Professional or trained person is required. Please take the necessary
precautions for handling all laboratory reagents.
3.The calibrator values are lot-specific with the matched models listed in the
value sheet.
4.Calibration is recommended after reagent lot change or execution of
specific maintenance or troubleshooting procedure.
5.Please perform scheduled maintenance and standard operation including
calibration and analysis to assure the performance of measurement
system.
6.Material safety data sheet is available on request.
7.Disposal of all waste material should be in accordance with local
guidelines.
Preparation
1.Take the vial out of the freezer and allow reaching room temperature.
2.According to the calibration procedure described in the instrument manual,
use the Calibrator value, Dilution factor and Predilution Calibrator
concentration listed in the value sheet to set calibration parameter and
Kalite kontrolü
Kalibrasyon durumunu izlemek için numune olarak Mindray kontrolünü
kullanın. Kontrol değer sayfasında gösterildiği üzere, kontrol sonucu
tanımlanan aralık dahilinde olmalıdır. Kontrol sonucu aralık dışındaysa ölçüm
sistemi kontrol edilmelidir. Örneğin analizöre yerleştirilen reaktif veya
numunenin konumu; kalibratörün son kullanma tarihi ve saklanma koşulları;
reaktif ve kontrol; yazılımdaki parametre ayarı veya analizör performansı.
Referanslar
1.ISO 17511:2003. In vitro diagnostic medical devices—Measurement of
quantities in biological samples—Metrological traceability of values
assigned to calibrators and control materials.
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