CueSee® Coag PT
Convenient and safe quality control for PT/INR with real coagulation factors, ideal for Proficiency Testing (PT).
Description
Eurotrol has revolutionized quality control for coagulation by developing CueSee Coag PT with real plasma performing like patient samples. Packaged in the CueSee® Mix, this innovative, dual-chambered device keeps the lyophilized plasma separated from the activation/reconsitution solution to provide a long shelf-life. This product is:
- Available in mutiple clinically relevant levels.
- Compatible with all common PT/INR point of care devices.
- Ideal for quality control, method comparisons, AMR validations and Proficiency Testing (PT)
Intended Use
Eurotrol CueSee® Coag PT is an unassayed, real plasma control intended for professional use in the verification of the precision and accuracy of Prothrombin Time (PT) and International Normalized Ratio (INR). The purpose of this quality control is to check calibration and other performance related characteristics.
Analytes
ARTICLE CODE
285.001.001
285.002.001
285.003.001
Level 1
Level 2
Level 3
INR
1.0 - 2.0
2.5 - 3.5
4.0 - 5.0
1
PT
-
-
-
s
ACT
-
-
-
s
All ranges per analyte are target ranges for manufacturing of the product. See actual value sheets with lot specific values, which may vary in range widths and mean values due to instrument chosen for value assignments.
Details
Container
Filling
Box
Storage Temperature
Shelf-life
CueSee® Mix
missing None.svg
1.6 ± 0.1 mL
1 per Box
Unopened
2 - 8 °C
Opened
20 - 25 °C
Unopened
> 3 months
Opened
5 min
Documents
Videos
CueSee® Coag Preparation