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
These are target ranges for manufacturing of the product. Individual lots have varying means and ranges due to a combination of factors, including assay method, instrument platform, reagent lot, matrix effects, etc. For accurate quality assessment and verification lot- specific values and ranges established by peer group results from CueSee® Compare should be used.

Details

CueSee® Mix
1.6 ± 0.1 mL
1 per Box
Unopened 2 - 8 °C
Opened 20 - 25 °C
Unopened > 3 months
Opened 5 min

Documents

Tutorials

CueSee® Coag Preparation