CueSee® CO-OXPT

Unique quality control for CO-oximeters with real hemoglobin derivatives for Proficiency Testing (PT).

CueSee® CO-OXPT

Unique quality control for CO-oximeters with real hemoglobin derivatives for Proficiency Testing (PT).

CueSee® CO-OXPT

Unique quality control for CO-oximeters with real hemoglobin derivatives for Proficiency Testing (PT).

CueSee® CO-OXPT

Unique quality control for CO-oximeters with real hemoglobin derivatives for Proficiency Testing (PT).

Description

Eurotrol has revolutionized quality control for CO-oximeters by developing CueSee CO-OX PT with real hemoglobin derivatives performing like patient samples. Packaged in the ACU-Drop® II, this innovative, dual-chambered device keeps the oxyhemoglobin separated from the methemoglobin to provide a long shelf-life. This product is:

- Available in 6 clinically relevant levels.

- Compatible with all common CO-oximeters.

- Ideal for quality control, method comparisons, AMR validations and proficiency testing.

Intended Use

Eurotrol CueSee® CO-OX PT is an unassayed, real hemoglobin control intended for professional use in the verification of the precision and accuracy of CO-oximeters measuring total hemoglobin (tHb) and fractions of Hb-derivatives Oxyhemoglobin (FO2Hb), Carboxyhemoglobin (FCOHb) and Methemoglobin (FMetHb). The purpose of this quality control is to check wavelength and absorbance calibration and other performance related characteristics.

Analytes

ARTICLE CODE
249.001.001
249.002.001
249.003.001
249.004.001
249.005.001
249.006.001
Level 1
Level 2
Level 3
Level 4
Level 5
Level 6
tHb
17.2 - 18.8
9.8 - 11.2
11.2 - 12.8
12.8 - 14.2
14.2 - 15.8
15.8 - 17.2
g/dL
O2Hb
85.0 - 100.0
75.0 - 85.0
65.0 - 75.0
55.0 - 65.0
45.0 - 55.0
35.0 - 45.0
%
COHb
2.5 - 7.5
7.5 - 12.5
12.5 - 17.5
17.5 - 22.5
22.5 - 27.5
27.5 - 32.5
%
MetHb
0.0 - 7.5
7.5 - 12.5
12.5 - 17.5
17.5 - 22.5
22.5 - 27.5
27.5 - 32.5
%
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

ACU-Drop® II
2.0 ± 0.1 mL
1 per Box
Unopened 2 - 8 °C
Opened 2 - 8 °C
Unopened N/A
Opened 15 minutes

Documents

Tutorials

CueSee® CO-OX
CueSee® CO-OX Preparation
ACU-Drop® II