The VisuCon-L Coag Screen Abnormal 1 is a hemostasis control plasma (Mid-Level Abnormal) that can be used in the quality control of quantitative coagulation assays, including Prothrombin Time (PT) and Activated partial thromboplastin time (APTT), in the mid-level abnormal range. The VisuCon-L Coag Screen ABN plasmas may be used with mechanical and photo-optical coagulation instruments in conjunction with appropriate commercial reagents. Good laboratory practice requires that assays be calibrated over the relevant range and that controls be performed regularly to confirm assay calibration. This plasma is citrated human plasma collected from a minimum of 20 donors, buffered with 0.05M HEPES buffer, as well as stabilizing agents, dispensed and lyophilized.
VisuCon-L Coag Screen Abnormal 1 is cleared for in vitro Diagnostic use by Health Canada and CE marked. They are available for sale in Canada and select European countries, not available in the United States.
Box containing 10 x 1 mL vials of lyophilized hemostasis control plasma (Mid-Level Abnormal), Prod. # LCSAB101
The results obtained with the VisuCon-L Coag Screen ABN plasmas will be subject to the limitations of the assay system including types of reagents and instrumentation.
Preparation/Handling:
Reconstitute each vial with 1 ml reagent grade water. Swirl gently and let stand for 15 minutes. Swirl gently once more before use.
Storage and Stability:
Vials are stable until the expiration date stated on the vial when stored at 2 – 8°C. Once reconstituted, the plasma is stable for 24 hours on-board (15 – 22°C) or at 2 – 8°C in original vial. Gently mix vial of plasma if left for more than 2 hours without use. Reconstituted material should be discarded after use and not be refrozen.
Assay Procedure:
After reconstituting the VisuCon-L Coag Screen ABN plasmas, use on coagulation instrument or assay system with corresponding reagents in accordance with established coagulation assay procedures. If appropriate control values are not obtained, assess the components of the assay system including reagents, substrate plasmas, calibrator plasma or instrumentation to try and identify potential sources of error.
UFNCP0125 – VisuCon-F Frozen Unassayed Normal Control Plasma – 25 x 1ml box (IVD) UFNCP0181 – VisuCon-F Frozen Unassayed Normal Control Plasma – 81 x 1ml box (IVD) UFNCP0481 – VisuCon-F Frozen Unassayed Normal Control Plasma – 81 x 4ml box (IVD)
Hemostasis Control Plasma (Mid-Level Abnormal)
LCSAB101 – VisuCon-L Coag Screen ABN1 – 10 x 1ml Box (IVD)
Description
Hemostasis Control Plasma (Mid-Level Abnormal)
The VisuCon-L Coag Screen Abnormal 1 is a hemostasis control plasma (Mid-Level Abnormal) that can be used in the quality control of quantitative coagulation assays, including Prothrombin Time (PT) and Activated partial thromboplastin time (APTT), in the mid-level abnormal range. The VisuCon-L Coag Screen ABN plasmas may be used with mechanical and photo-optical coagulation instruments in conjunction with appropriate commercial reagents. Good laboratory practice requires that assays be calibrated over the relevant range and that controls be performed regularly to confirm assay calibration. This plasma is citrated human plasma collected from a minimum of 20 donors, buffered with 0.05M HEPES buffer, as well as stabilizing agents, dispensed and lyophilized.
VisuCon-L Coag Screen Abnormal 1 is cleared for in vitro Diagnostic use by Health Canada and CE marked. They are available for sale in Canada and select European countries, not available in the United States.
The results obtained with the VisuCon-L Coag Screen ABN plasmas will be subject to the limitations of the assay system including types of reagents and instrumentation.
Preparation/Handling:
Reconstitute each vial with 1 ml reagent grade water. Swirl gently and let stand for 15 minutes. Swirl gently once more before use.
Storage and Stability:
Vials are stable until the expiration date stated on the vial when stored at 2 – 8°C. Once reconstituted, the plasma is stable for 24 hours on-board (15 – 22°C) or at 2 – 8°C in original vial. Gently mix vial of plasma if left for more than 2 hours without use. Reconstituted material should be discarded after use and not be refrozen.
Assay Procedure:
After reconstituting the VisuCon-L Coag Screen ABN plasmas, use on coagulation instrument or assay system with corresponding reagents in accordance with established coagulation assay procedures. If appropriate control values are not obtained, assess the components of the assay system including reagents, substrate plasmas, calibrator plasma or instrumentation to try and identify potential sources of error.
Product Datasheet: VisuCon-L Coag Screen ABN1 - Freeze Dried Mid-Level Abnormal Plasma
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