Your D-Dimer Quality Controls play an essential role to validate the test system's performance:
- Check the accuracy and reliability of results reported by your D-Dimer testing system for all patient samples on a daily basis
- Evaluate the precision in various operating conditions
- Monitor the consistency of results over a prolonged period of time
- Comply with quality management recommendations.
Stago offers a reliable, fully automated, ready-to-use testing system with STA®-Liatest® D-Di Plus and STA®-D-Di Control.
STA®-D-Di Control are:
Compliant with international quality management recommendations
2 assayed quality controls located at ideal levels:
Control 1 ~ 0.75 µg/mL FEU
Control 2~ 2.30 µg/mL FEU
Adapted to your day-to-day D-Dimer testing activity
- Liquid, ready-to-use: convenient for minimising handling procedures errors
- Extended stability: 72h on board STA-R® and STA Compact®, stable for 15 days after opening when stored at 2-8°C
- 2 mL vials: allows several QC runs per day
A key component of your system thanks to barcode-based management of product data
- Autopopulation of dedicated ranges guarantees the safety of the system
- Optimal management of volumes, stability, expiry dates, batch numbers etc
STA®-D-Di Control - Cat. Nr. 00868
Packaging 2 x 6 x 2 mL - Liquid
On-board stability: 72h on STA-R® and STA Compact®
Stability at 2-8°C: 15 days
Associated reagents:
- STA®-Liatest® D-Di Plus* - Cat. Nr. 00662
- STA®-Liatest® D-Di - Cat. Nr 00515
Associated D-Di EQA program Qualiris QC D-Dimer** - Cat. Nr 01049
* Not available in USA and Canada.
** QC availability depending on the program subscription