CYANSmart App Sheets ENG
CYANSmart App Sheets ENG
English
CYANSmart
Application Sheets
ISO 13485-2016
www.diagnostics.be • Belgium • Tel: ++ 32 15 67 67 68 • e-mail: cypress@diagnostics.be
Layout 20181024
DIRECTIONS FOR USE
AUTOMATION
CYANSmart
CLINICAL CHEMISTRY
REF HBE03
α-Amylase
VOL 20 x 2 ml
Kinetic-colorimetric test
Standard - With CNPG3
After opening the reagent is stable for 60 days when properly capped immediately after each opening and stored at 2°-8°C. The
reagent should be discarded if turbidity or precipitation has occurred or if the blank absorbance is out of range².
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample³ (Calibrator1)
(Calibrator1) 20 µl
Sample 20 µl³
Reagent 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
3
These values are for serum or plasma samples. For urine samples; use 10 µl of sample, Normal High: 450 and Factor: 7908.
4
The control values can be found on the control sheets delivered together with the control vials.
LINEARITY
This method is linear up to 2200 U/l of α-amylase.
If the obtained results are greater than 2200 U/l, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HBE01
Acid Phosphatase Total
VOL 18 x 2 ml
Colorimetric kinetic test
Standard - α -Naphthyl phosphate. Hillmann
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature. Then, pipette into a test tube:
Blank² Sample (Calibrator1)
(Calibrator1) 100 µl
Sample 100 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials.
LINEARITY
This method is linear up to 150 U/L of Acid Phosphatase.
If the obtained results are greater than 150 U/l, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HBE01
Acid Phosphatase (Non) Prostatic
VOL 18 x 2 ml
Colorimetric kinetic test
Standard - α-Naphthyl phosphate. Hillmann.
REAGENT PREPARATION AND STABILITY, CALIBRATION & QUALITY CONTROL & LINEARITY
see ACPt. (Page 4)
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
1
(Calibrator ) 100 µl
Sample 100 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Reagent 3 10 µl 10 µl 10 µl
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator).
Wait with the preparation of the next sample until the CYANSmart is finished with measuring the previous one. At this time, the
CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials.
NOTES
To obtain a value for Prostatic Acid Phosphatase (ACPp), you can calculate the ratio: ACPp = ACPt – ACPnp.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
Standard1 5 µl
Sample 5 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Then, incubate for 10 minutes at room temperature. After the incubation time,
aspirate and measure all the samples within one hour after preparation.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
4
The control values can be found on the control sheets delivered together with the control vials.
LINEARITY
This method is linear up to 5.8 g/dl of Albumin.
If the obtained results are greater than 5.8 g/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HBE02
Alkaline Phosphatase (ALP)
VOL 15 x 15 ml
Kinetic test optimized (DGKC)
Standard -
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
(Calibrator1) 15 µl
Sample 15 µl
Working solution (R1 + R2) 0.9 ml 0.9 ml 0.9 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials.
LINEARITY
This method is linear up to 1200 U/l of Alkaline Phosphatase.
If the obtained results are greater than 1200 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and multiply
the result by factor 10.
REF HBE12
Alkaline Phosphatase Liquid
VOL 60 + 15 ml
Kinetic. Colorimetric. IFCC
Standard -
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
(Calibrator1) 20 µl
Sample 20 µl
Working solution (R1 + R2) 1 ml 1 ml 1 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials.
LINEARITY
This method is linear up to 1400 U/l of Alkaline Phosphatase.
If the obtained results are greater than 1400 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and multiply
the result by factor 10.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature, protect samples from direct sunlight.
Then, pipette into a test tube:
Blank Sample Blank Sample Calibrator1 Blank Calibrator1
Calibrator1 100 µl 100 µl
Sample 100 µl 100 µl
Reagent N 25 µl 25 µl
Reagent D 750 µl 750 µl 750 µl 750 µl 750 µl
Thus, for every sample, you need to prepare 2 test tubes: one for measuring the sample blank (background coloration) and one for
measuring the real sample coloration. Add Reagent N only to the second tube. Add Reagent D last, mix and incubate for exactly 5
minutes at room temperature. Aspirate the mixture in the CYANSmart, exactly 5 minutes after addition of the Reagent D.
Use the pictures on page 11-12 as guidance.
PROGRAM SETUP
Program Name: BILD Blank Low: 0.00002
Program Method: End Point Blank High: 0.10002
Main Filter: 546 Normal Low: 0.0600 mg/dL
Sub Filter: None Normal High: 0.2500 mg/dL
1
Program Unit: mg/dL Num of STD: 0
Aspiration Volume: 0500 µl CONC: 0.00001 mg/dL
Delay Time: 001 sec Factor: 19.0000
Test Time: 003 sec Control N Min: 0.00004 mg/dL
Dilution Factor: 1.0000 Control N Max: 0.00004 mg/dL
4
Linearity Min: 0.0600 mg/dL Control P Min: 0.0000 mg/dL
Linearity Max: 20.0000 mg/dL Control P Max: 0.00004 mg/dL
Blank: Serum² Cuvette Temp: 37 °C
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
²The Blank method programmed is Serum. ! Pay attention, this determines the calculation of the results, not the blank aspiration!
1. Aspirate distilled water to adjust the instrument to zero (AD value)
2. “Test Blank” “yes” and aspirate Reagent D (blank)
3. In the standard/sample menu,
a. First: “Aspirate Serum” = Standard/Sample Blank.
b. Secondly: “Aspirate Standard/Sample” = Standard/Sample (including 25 µl of RN).
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 20 mg/dl of Bilirubin Direct. If the obtained results are greater than 20 mg/dl, dilute the sample 1:2 with
saline solution, repeat the determination, and multiply the result by factor 2.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature, protect samples from direct sunlight. Then, pipette into a test tube:
Blank Sample Blank Sample Calibrator1 Blank Calibrator1
1 100 µl 100 µl
Calibrator
Sample 100 µl 100 µl
Reagent N 25 µl 25 µl
Reagent T 750 µl 750 µl 750 µl 750 µl 750 µl
Thus for every sample, you need to prepare 2 test tubes: one for measuring the sample blank (background coloration) and one for
measuring the real sample coloration. Add Reagent N only to the second tube. Add Reagent T last, mix and incubate for exactly 5
minutes at room temperature. Aspirate the mixture in the CYANSmart, exactly 5 minutes after addition of the Reagent T.
Use the pictures on page 11-12 as guidance.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² The Blank method programmed is Serum. ! Pay attention, this determines the calculation of the results, not the blank aspiration!
1. Aspirate distilled water to adjust the instrument to zero (AD value)
2. “Test Blank” “yes” and aspirate Reagent T (blank)
3. In the standard/sample menu,
a. First: “Aspirate Serum” = Standard/Sample Blank.
b. Secondly: “Aspirate Standard/Sample” = Standard/Sample (including 25 µl of RN).
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 20 mg/dl of Bilirubin total. If the obtained results are greater than 20 mg/dl, dilute the sample 1:2 with
saline solution, repeat the determination, and multiply the result by factor 2.
Cypress Diagnostics: Nijverheidsstraat 8 • 2235 Hulshout • Belgium • www.diagnostics.be • Tel: ++ 32 15 67 67 68 • e-mail: cypress@diagnostics.be
CY009 CYANSmart
Application sheet
Cypress Diagnostics: Nijverheidsstraat 8 • 2235 Hulshout • Belgium • www.diagnostics.be • Tel: ++ 32 15 67 67 68 • e-mail: cypress@diagnostics.be
CY009 CYANSmart
Application sheet
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
Standard1 20 µl
Sample 20 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 2 minutes at 15-25°C. After the incubation time, aspirate
and measure all the samples within one hour after preparation.
PROGRAM SETUP
Num of Blank: 3
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
3
These values are for serum or plasma samples. For urine samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 20 mg/dl of Calcium.
If the obtained results are greater than 20 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HB005
Chloride
VOL 2 x 125 ml
Thiocyanate. Colorimetric
Standard 1 x 5 ml
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
Standard1 10 µl
Sample 10 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 5 minutes at 37°C/15-25°C. After the incubation time,
aspirate and measure all the samples within 30 minutes after preparation.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
3
These values are for serum or plasma samples. For urine samples; please check the insert for the values and sample preparation
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 190 mmol/l of Chloride.
If the obtained results are greater than 190 mmol/l, dilute the sample 1:2 with distilled water, repeat the determination, and
multiply the result by factor 2.
REF HB006
Cholesterol Lyophilized
VOL 2 x 125 ml
Enzymatic. Colorimetric test (CHOD-POD)
Standard 1 x 5 ml
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
1
Standard 10 µl
Sample 10 µl
Working reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate 15 minutes at 15-25°C or 10 min at 37°C. After the incubation
time, aspirate and measure all the samples within 45 minutes after preparation.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 900 mg/dl of Cholesterol.
If the obtained results are greater than 900 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
Standard1 10 µl
Sample 10 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate 15 minutes at 15-25°C or 10 minutes at 37°C. After the
incubation time, aspirate and measure all the samples within 45 minutes after preparation.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 1000 mg/dl of Cholesterol.
If the obtained results are greater than 1000 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and
multiply the result by factor 2.
REF HBL011
HDL Cholesterol Direct
VOL 40 + 120 ml
Enzymatic Colorimetric
Standard -
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature. Then, pipette into a test tube:
Reagent Blank² Calibrator Blank1 Calibrator1 Sample Blank Sample
1
Calibrator 10 µl 10 µl
Sample 10 µl 10 µl
Distilled water 10 µl
R1 750 µl 750 µl 750 µl 750 µl 750 µl
Mix and incubate for exactly 5 minutes at 37°C. And then add:
R2 250 µl - 250 µl - 250 µl
Mix and incubate for exactly 5 minutes at 37°C. And then aspirate.
Thus, for every sample, you need to prepare 2 test tubes: one for the Calibrator/Sample Blank, to measure the background
coloration caused by the sample, and one for the Calibrator/Sample to measure the coloration caused by the reaction. After mixing
Calibrator/Sample and R1, incubate at 37°C for exactly 5 minutes. Then add R2 only to the Calibrator/Sample tube, mix and
incubate for another 5 minutes at 37°C. Then aspirate the mixtures in the CYANSmart to measure exactly 10 minutes after adding
R1. You can prepare several samples simultaneously as long as you respect the times mentioned.
Use the illustrations p.19 for guidance to perform this test in a time-efficient way.
PROGRAM SETUP
Program Name: HDLd Blank Low: 0.00002
Program Method: End Point Blank High: 1.0000²
Main Filter: 578 Normal Low: 59.0000 mg/dL
Sub Filter: None Normal High: 80.0000 mg/dL
Program Unit: mg/dL Num of STD: 1
Aspiration Volume: 0500 µl CONC: (value see vial)1 mg/dL
Delay Time: 001 sec Factor: 0.0000
Test Time: 003 sec Control N Min: 0.00004 mg/dL
Dilution Factor: 1.0000 Control N Max: 0.00004 mg/dL
4
Linearity Min: 1.0600 mg/dL Control P Min: 0.0000 mg/dL
Linearity Max: 184.8000 mg/dL Control P Max: 0.00004 mg/dL
Blank: Serum² Cuvette Temp: 37 °C
Num of Blank: 1
1
Enter the concentration values shown on the calibrator vials (HBC11)
² The Blank method programmed is Serum! Pay attention, this determines the calculation of the results, not the blank aspiration!
1. Aspirate distilled water to adjust the instrument zero (AD value)
2. “Test Blank” “YES” and aspirate the Reagent Blank (R1 + R2 + Water)
3. In the Calibrator/Sample menu:
a. “Aspirate Serum” = Calibrator/Sample Blank mixture (Calibrator/Sample + R1)
b. “Aspirate Standard/Sample” = Calibrator/sample mixture (Calibrator/Sample + R1 + R2)
4
The control values can be found on the labels of the HDL/LDL Direct control set vials (HBC10)
LINEARITY
This method is linear up to 184.8 mg/dl of HDL Cholesterol. If the obtained results are greater than 184.8 mg/dl, dilute the sample
1:2 with saline solution, repeat the determination, and multiply the result by factor 2.
REF HBL012
LDL Cholesterol Direct
VOL 40 + 120 ml
Enzymatic Colorimetric
Standard -
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature. Then, pipette into a test tube:
Reagent Blank² Calibrator Blank1 Calibrator1 Sample Blank Sample
Calibrator 10 µl 10 µl
Sample 10 µl 10 µl
Distilled water 10 µl
R1 750 µl 750 µl 750 µl 750 µl 750 µl
Mix and incubate for exactly 5 minutes at 37°C. And then add:
R2 250 µl 250 µl 250 µl
Mix and incubate for exactly 5 minutes at 37°C. And then aspirate.
Thus for every sample, you need to prepare 2 test tubes: one for the Calibrator/Sample Blank, to measure the background
coloration caused by the sample, and one for the Calibrator/Sample to measure the coloration caused by the reaction. After mixing
Calibrator/Sample and R1, incubate at 37°C for exactly 5 minutes. Then add R2 only to the Calibrator/Sample tube, mix and
incubate for another 5 minutes at 37°C. Then aspirate the mixtures in the CYANSmart to measure exactly 10 minutes after adding
R1. You can prepare several samples simultaneously as long as you respect the times mentioned.
Use the illustrations p19 for guidance to perform this test in a time-efficient way.
PROGRAM SETUP
Program Name: LDLd Blank Low: 0.00002
Program Method: End Point Blank High: 1.0000²
Main Filter: 578 Normal Low: 50.00000 mg/dL
Sub Filter: None Normal High: 100.0000 mg/dL
Program Unit: mg/dL Num of STD: 1
Aspiration Volume: 0500 µl CONC: (value see vial) 1 mg/dL
Delay Time: 001 sec Factor: 0.0000
Test Time: 003 sec Control N Min: 0.00004 mg/dL
Dilution Factor: 1.0000 Control N Max: 0.00004 mg/dL
Linearity Min: 1.6400 mg/dL Control P Min: 0.00004 mg/dL
4
Linearity Max: 250.0000 mg/dL Control P Max: 0.0000 mg/dL
Blank: Serum² Cuvette Temp: 37 °C
Num of Blank: 1
1
Enter the concentration values shown on the calibrator vials (HBC11)
² The Blank method programmed is Serum! Pay attention, this determines the calculation of the results, not the blank aspiration!
1. Aspirate distilled water to adjust the instrument zero (AD value)
2. “Test Blank” “YES” and aspirate the Reagent Blank (R1 + R2 + Water)
3. In the Calibrator/Sample menu:
a. “Aspirate Serum” = Calibrator/Sample Blank mixture (Calibrator/Sample + R1)
b. “Aspirate Standard/Sample” = Calibrator/sample mixture (Calibrator/Sample + R1 + R2)
4 The control values can be found on the labels of the HDL/LDL Direct control set vials (HBC10)
LINEARITY
This method is linear up to 250.0 mg/dl of LDL Cholesterol. If the obtained results are greater than 250.0 mg/dl, dilute the sample
1:2 with saline solution, repeat the determination, and multiply the result by factor 2.
Cypress Diagnostics: Nijverheidsstraat 8 • 2235 Hulshout • Belgium • www.diagnostics.be • Tel: ++ 32 15 67 67 68 • e-mail: cypress@diagnostics.be
CY009 CYANSmart
Application sheet
REF HBE10
Creatine Kinase MB
VOL 19 x 2,5 ml
Immunoinhibition. Kinetic UV
CK control 1 x 2 ml
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank1 Sample (Calibrator)
1
(Calibrator ) 40 µl
Sample 40 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
2
Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 1000 U/l of CK-NAC (CK-MB is between 6 and 25% of total CK activity).
If the obtained results are greater than 1000 U/l for CK-NAC, dilute the sample 1:2 with saline solution, repeat the determination,
and multiply the result by factor 2.
REF HBEL05
Creatine Kinase MB Liquid
VOL 60 + 15 ml
Immunoinhibition. Kinetic UV
CK control 1 x 2 ml
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank1 Sample (Calibrator)
1
(Calibrator ) 40 µl
Sample 40 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
2
Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 318 U/l of CK-MB.
If the obtained results are greater than 318 U/l, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HBE04
Creatine Kinase NAC
VOL 20 x 2,5 ml
Kinetic UV. NAC Activated
Standard -
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
(Calibrator1) 20 µl
Sample 20 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 1300 U/l of CK-NAC.
If the obtained results are greater than 1300 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and multiply
the result by factor 10.
REF HBEL03
Creatine Kinase NAC Liquid
VOL 60 + 15 ml
Kinetic UV. NAC Activated
Standard -
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
(Calibrator1) 20 µl
Sample 20 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 2000 U/l of CK-NAC.
If the obtained results are greater than 2000 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and multiply
the result by factor 10.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample Standard1
Standard1 100 µl
Sample 100 µl
Working reagent (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
3
These values are for serum or plasma samples. For urine samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 15 mg/dl of Creatinine.
If the obtained results are greater than 15 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HBE11
G6-PDH
VOL 100 + 20 ml
U.V. Enzymatic
Standard -
SAMPLE PREPARATION
1. PREPARATION for ERYTHROCYTES
Wash 0,2 ml of blood with 2 ml of 0.9% NaCl (saline) solution. Centrifuge after each wash for 10 min at around 3000 rpm. Repeat 3
times. Suspend the washed and centrifuged erythrocytes in 0,5 ml of R4 and let stand for 15 min at +4°C and then centrifuge again.
Use the supernatant in the assay within 2 hours.
2. TEST STEP for ERYTHROCYTES
Make sure the reagents and samples are at room temperature. Then, pipette into a test tube:
Sample
Hemolysate 15 µl
Reagent 1 1.0 ml
Reagent 2 30 µl
Mix and incubate for 5 min at 37°C, then add:
Reagent 3 15 µl
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample. Wait with the preparation of the next sample until the CYANSmart is finished with measuring the
previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
3
These values are for erythrocytes (U/L). To obtain results in U/g HGB, divide the results of this analysis with the results for
Hemoglobin (g/L) for that sample.
4
The control values can be found on the control vials
LINEARITY
This method is linear up to 4303 U/L of G6-PDH.
If the obtained results are greater than 4303 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and
multiply the result by factor 10.
REF HB009
Glucose Lyophilized
VOL 2 x 125 ml
Enzym Enzymatic. Colorimetric
Standard - GOD-POD
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature. Then, pipette into a test tube:
Blank Sample Standard1
1
Standard 10 µl
Sample 10 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 10 min at 37°C or 20 minutes at 15-25°C.
After the incubation time, aspirate and measure all the samples within 30 minutes.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
3
These values are for serum or plasma samples. For CSF samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 500 mg/dl of Glucose.
If the obtained results are greater than 500 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
1
Standard 10 µl
Sample 10 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 15 min at 37°C. After the incubation time, aspirate and
measure all the samples within 45 minutes.
PROGRAM SETUP
Program Name: GLUCL Blank Low: 0.00002
Program Method: End Point Blank High: 0.32002
Main Filter: 510 Normal Low: 60.0000³ mg/dL
Sub Filter: None Normal High: 110.0000³ mg/dL
Program Unit: mg/dL Num of STD: 1
Aspiration Volume: 0500 µl CONC: 100.00001 mg/dL
Delay Time: 001 sec Factor: 0.0000
Test Time: 003 sec Control N Min: 0.00004 mg/dL
Dilution Factor: 1.0000 Control N Max: 0.0000 4 mg/dL
Linearity Min: 1.1800 mg/dL Control P Min: 0.00004 mg/dL
Linearity Max: 600.0000 mg/dL Control P Max: 0.0000 4 mg/dL
Blank: Reagent Cuvette Temp: 37 °C
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
3
These values are for serum or plasma samples. For CSF samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 600 mg/dl of Glucose.
If the obtained results are greater than 600 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HBL04 HBL04A HBL04M New formulation starting from lot GL-00731
VOL 2 x 125 ml 8 x 125 ml 8 x 30 ml
Glucose Liquid
Standard 1 x 5 ml 4 x 5 ml -
Enzymatic. Colorimetric. GOD-POD
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
Standard1 10 µl
Sample 10 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 10 min at 37°C or 15 min at 15-25°C.
After the incubation time, aspirate and measure all the samples within 40 minutes.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 460 mg/dl of Glucose.
If the obtained results are greater than 460 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HBE05
γ-GT
VOL 15 x 15 ml
(Gamma-Glutamyl-Transferase)
Standard - Kinetic test. Carboxy substrate
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
(Calibrator1) 100 µl
Sample 100 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 375 U/L of γ-GT.
If the obtained results are greater than 375 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and multiply
the result by factor 10.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
(Calibrator1) 100 µl
Sample 100 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 300 U/L of γ-GT.
If the obtained results are greater than 300 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and multiply
the result by factor 10.
REF HBE06
GOT (AST)
VOL 15 x 15 ml
U.V. Kinetic test
Standard - According IFCC
The reagent should be discarded if turbidity or precipitation has occurred or if the blank absorbance is out of range².
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
(Calibrator1) 100 µl
Sample 100 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 360 U/L of GOT.
If the obtained results are greater than 360 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and multiply
the result by factor 10.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
1
(Calibrator ) 100 µl
Sample 100 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control vials
LINEARITY
This method is linear up to 260 U/L of GOT.
If the obtained results are greater than 260 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and multiply
the result by factor 10.
REF HBE07
GPT (ALT)
VOL 15 x 15 ml
U.V. Kinetic test
Standard - According to IFCC
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
(Calibrator1) 100 µl
Sample 100 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Program Name: GPT Blank Low: 1.00002
Program Method: Kinetic Blank High: 2.50002
Main Filter: 340 Normal Low: 0.0000 U/L
Sub Filter: None Normal High: 40.0000 U/L
Program Unit: U/L Num of STD: 01
Aspiration Volume: 0500 µl CONC: 0.00001 U/L
1
Delay Time: 060 sec Factor: 1750.0000
Test Time: 090 sec Control N Min: 0.00004 U/L
4
Dilution Factor: 1.0000 Control N Max: 0.0000 U/L
Linearity Min: 0.0000 U/L Control P Min: 0.00004 U/L
4
Linearity Max: 400.0000 U/L Control P Max: 0.0000 U/L
Blank: Reagent2 Cuvette Temp: 37 °C
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 400 U/L of GPT.
If the obtained results are greater than 400 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and multiply
the result by factor 10.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
1
(Calibrator ) 100 µl
Sample 100 µl
Working solution (R1 + R2) 1.0 ml 1.0 ml 1.0 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 260 U/L of GPT.
If the obtained results are greater than 260 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and multiply
the result by factor 10.
REF HT001
HbA c1
VOL 30 x 10 ml
Turbidimetric
Standard -
SAMPLE PREPARATION
1. Precipitation
To determine HbA1c, a hemolysate must be prepared for each sample as well as for Calibrator HT001S (Level 1 to 4) and Control
HT001C:
- Dispense 1 mL of Reagent 3 into labeled test tubes (glass or plastic). Also provide test tubes for Calibrator and Control.
- Add 20 μL of well mixed whole blood (sample, calibrator, control). Mix.
- Allow to stand for 5 minutes or until complete lysis is evident. Hemolysates may be stored up to 10 days at 2-8°C.
2. Test step
Make sure the samples and reagents are at room temperature. Then, pipette into a test tube:
Blank Sample Calibrators
Calibrators (hemolysed) 15 µl
Sample (hemolysed) 15 µl
Reagent 1 540 µl 540 µl 540 µl
Mix and incubate for exactly 5 min at 37°C. And then add:
Reagent 2 180 µl 180 µl 180 µl
Mix and incubate for exactly 5 min at 37°C. And then aspirate:
You can prepare several samples simultaneously, as long as you respect the times mentioned!
PROGRAM SETUP
Program Name: HbA1c Normal Low: 2.0000 %
Program Method: End Point Normal High: 6.0000 %
Main Filter: 620 Num of STD: 5
Sub Filter: None STD 1 CONC: 0.0010 %
Program Unit: % STD 2 CONC: * (=CAL 1) %
Aspiration Volume: 0500 µl STD 3 CONC: * (=CAL 2) %
Delay Time: 001 sec STD 4 CONC: * (=CAL 3) %
Test Time: 003 sec STD 5 CONC: * (=CAL 4) %
Dilution Factor: 1.0000 Factor: 0.0000
Linearity Min: 2.0000 % Control N Min: 0.00004 %
Linearity Max: 16.0000 % Control N Max: 0.00004 %
4
Blank: Reagent Control P Min: 0.0000 %
REF HB011
Hemoglobin
VOL 4 x 5 ml
Drabkin
Standard - Colorimetric test
All the components of the kit and the hemoglobin calibrator (HBS02) are stable at 2-8°C up to the date of expiration as specified,
when stored tightly closed, protected from light and contaminations prevented during their use.
The reagent should be discarded if turbidity or precipitation has occurred or if the blank absorbance is out of range².
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Calibrator1
Calibrator1 10 µl
Sample 10 µl
Working reagent 2.5 ml 2.5 ml 2.5 ml
Mix and incubate for 3 minutes at room temperature 15-25°C, then aspirate to measure. You can prepare several samples
simultaneously, as long as you respect the times mentioned!
PROGRAM SETUP
Num of Blank: 1
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 20 g/dl of Hemoglobin.
If the obtained results are greater than 20 g/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HB012
Iron
VOL 4 x 50 ml
Colorimetric test. ‘‘Ferrozine’’
Standard 1 x 10 ml
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature. Then, pipette into a test tube:
Reagent Blank Sample Blank Sample Standard Blank1 Standard1
Standard 200 µl 200 µl
Sample 200 µl 200 µl
Distilled Water 200 µL
Working reagent (R1+R2) 1.0 ml 1.0 ml 1.0 ml 1.0 ml 1.0 ml
Reagent 3 1 drop 1 drop 1 drop
Mix and incubate for 10 minutes at 15-25°C. After the incubation time, aspirate and measure all the samples within 30 min after
preparation.
Thus, for every sample, you need to prepare 2 test tubes: one for measuring the sample blank (background coloration) and one for
measuring the real sample coloration.
PROGRAM SETUP
REF HB017
TIBC
VOL 100 tests
(Total Iron Binding Capacity).
Standard - Saturation and precipitating reagents.
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned on the insert
provided with HBC03.
2
The Blank method programmed is Serum. ! Pay attention, this determines the calculation of the results, not the blank aspiration!
- Aspirate distilled water to adjust the instrument to zero (AD value)
- “Test Blank” “yes” and aspirate Reagent Blank mixture
- In the standard/sample menu,
a. First: “Aspirate Serum” = Standard/Sample Blank.
b. Secondly: “Aspirate Standard/Sample” = Standard/Sample (including 1 drop of R3).
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 1000 µg/dl of Iron. If the obtained results are greater than 1000 µg/dl, dilute the sample 1:2 with saline
solution, repeat the determination, and multiply the result by factor 2.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample (Calibrator1)
(Calibrator1) 15 µl
Sample 15 µl
Working solution (R1 + R2) 0.9 ml 0.9 ml 0.9 ml
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Num of Blank: 1
1
Calibration by means of a Factor. Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of
STD: 1 and CONC: as mentioned on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 1600 U/L of LDH.
If the obtained results are greater than 1600 U/l, dilute the sample 1:10 with saline solution, repeat the determination, and
multiply the result by factor 10.
REF HBE09
Lipase
VOL 4 x 10 ml
Enzymatic. Colorimetric.
Calibrator 1 vial (Lyo.)
Calibrator: Reconstitute the contents of one vial with 1 mL of distilled water. Mix gently until complete solution.
Stability: 7 days at 2-8ºC. Divide standard solution into small volumes and freeze. Stability: 3 months at -20ºC.
All the components of the kit are stable at 2-8°C up to the date of expiration as specified, when stored tightly closed, protected
from light and contaminations prevented during their use.
R1 should be discarded if turbidity or precipitation has occurred or if the blank absorbance is out of range². R2 is a turbid orange-
colored micro-emulsion, discard if turning red.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank² Sample Calibrator1
Distilled water 10 µl
Calibrator1 10 µl
Sample 10 µl
Reagent 1 1.0 ml 1.0 ml 1.0 ml
Reagent 2 200 µl 200 µl 200 µl
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”.
PROGRAM SETUP
Program Name: LIPASE Blank Low: 0.00002
Program Method: Kinetic Blank High: 1.40002
Main Filter: 578 Normal Low: 5.0000 U/L
Sub Filter: None Normal High: 38.0000 U/L
1
Program Unit: U/L Num of STD: 1
Aspiration Volume: 0500 µl CONC: (value see insert)1 U/L
1
Delay Time: 060 sec Factor: 0.0000
Test Time: 090 sec Control N Min: 0.00004 U/L
4
Dilution Factor: 1.0000 Control N Max: 0.0000 U/L
Linearity Min: 5.0000 U/L Control P Min: 0.00004 U/L
4
Linearity Max: 250.0000 U/L Control P Max: 0.0000 U/L
Blank: Reagent2 Cuvette Temp: 37 °C
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively,
you can program and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 250 U/L of Lipase. If the obtained results are greater than 250 U/l, dilute the sample 1:10 with saline
solution, repeat the determination, and multiply the result by factor 10.
SAMPLE PREPARATION
Make sure the reagent and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
Standard1 10 µl
Sample 10 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 5 minutes at 15-25° or 3 min at 37°C. After the incubation
time, aspirate and measure all the samples within 45 min after preparation.
PROGRAM SETUP
Num of Blank: 3
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
3
These values are for serum or plasma samples. For urine samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 6.6 mg/dl of Magnesium.
If the obtained results are greater than 5 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HB014
Phosphorus
VOL 2 x 125 ml
U.V.-test. Phosphmolybdate
Standard 1 x 5 ml
AMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
1
Standard 10 µl
Sample 10 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
Mix and incubate for 5 minutes at 37°C. After the incubation time, aspirate and measure the sample.
You can prepare several samples simultaneously, as long as you respect the time mentioned!
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
3
These values are for serum or plasma samples. For urine samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 35 mg/dl of Phosphorus.
If the obtained results are greater than 35 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HB015
Potassium
VOL 3 x 50 ml
Colorimetric test. NaTPB
Standard 1 x 3 mL
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature. Then, pipette into a test tube:
Sample
Sample 50 µl
Reagent 3 500 µl
Mix carefully. Centrifuge for 5-10 min at 5000 rpm. Collect the supernatant in a new test tube:
Blank Sample Standard1
Standard1 100 µl
Supernatant 100 µl
Working Reagent (R1+R2) 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. To produce a homogeneous turbidity, the standard or the clear supernatant
must be added to the center of the surface of the working reagent in the test tube. Mix each test tube carefully before proceeding
to the next sample. Mix and allow for stand for 5 min. After the incubation time, aspirate and measure all the samples within 30
min after addition of the working solution.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
3
These values are for serum samples. For plasma samples; please check the insert for the values
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 10 mEq/l of Potassium.
If the obtained results are greater than 10 mEq/l, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HB016
Sodium
VOL 1 x 60 ml
Colorimetric test. Mg-Uranylacetate
Standard 1 x 2 mL
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature. Then, pipette into a test tube:
Blank Sample Standard1
1
Standard 20 µl
Sample 20 µl
Reagent 2 1.0 ml 1.0 ml
Mix well. Incubate for 5 min. Then shake intensively for at least 30 sec. Then incubate for 30 min.
Centrifuge for 5-10 min at 5000 rpm. Collect the supernatant in a new test tube:
Blank Sample Standard1
Reagent 2 20 µl
Supernatant 20 µl 20 µl
Reagent 1 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 5 minutes at room temperature. After the incubation time,
aspirate and measure all the samples within 30 min after addition of the reagent 1.
PROGRAM SETUP
Program Name: SOD Blank Low: 0.0000
Program Method: End Point Blank High: 2.5000
Main Filter: 405 Normal Low: 135.0000 mEq/L
Sub Filter: None Normal High: 155.0000 mEq/L
Program Unit: mEq/L Num of STD: 1
Aspiration Volume: 0500 µl CONC: 150.00001 mEq/L
Delay Time: 001 sec Factor: 0.0000
Test Time: 003 sec Control N Min: 0.00004 mEq/L
Dilution Factor: 1.0000 Control N Max: 0.00004 mEq/L
Linearity Min: 49.0000 mEq/L Control P Min: 0.0000 4 mEq/L
Linearity Max: 300.0000 mEq/L Control P Max: 0.00004 mEq/L
Blank: Reagent Cuvette Temp: 37 °C
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 300 mEq/l of Sodium.
If the obtained results are greater than 300 mEq/l, dilute the sample 1:2 with distilled water, repeat the determination, and multiply
the result by factor 2.
REF HB018
Total lipids
VOL 2 x 125 ml
Colorimetric test
Standard 1 x 5 mL Phosphovainilla
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard
Standard 100 µl
Sample 100 µl
Sulphuric acid 2.5 ml 2.5 ml
Shake thoroughly using a mechanical stirrer. Incubate for 10 min in a boiling water bath (100°C).
After that, cool in iced water and transfer into a new test tube:
Blank Sample Standard
Standard acid digest 50 µl
Sample acid digest 50 µl
Reagent 1 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Shake thoroughly using a mechanical stirrer. Incubate for 15 minutes at 37°C.
After the incubation time, aspirate and measure all the samples within 1 hour after addition of the reagent 1.
PROGRAM SETUP
Num of Blank: 1
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 1500 mg/dl of lipids.
If the obtained results are greater than 1500 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and
multiply the result by factor 2.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
1
Standard 25 µl
Sample 25 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 10 minutes at 15-25°C or 5 min at 37°C. After the incubation
time, aspirate and measure all the samples within one hour after preparation.
PROGRAM SETUP
Program Name: TP Blank Low: 0.00002
Program Method: End Point Blank High: 0.22002
Main Filter: 546 Normal Low: 6.6000 g/dL
Sub Filter: None Normal High: 8.3000 g/dL
Program Unit: g/dL Num of STD: 1
Aspiration Volume: 0500 µl CONC: (value see vial)1 g/dL
Delay Time: 001 sec Factor: 0.0000
Test Time: 003 sec Control N Min: 0.00004 g/dL
4
Dilution Factor: 1.0000 Control N Max: 0.0000 g/dL
Linearity Min: 0.0080 g/dL Control P Min: 0.00004 g/dL
Linearity Max: 15.0000 g/dL Control P Max: 0.00004 g/dL
Blank: Reagent Cuvette Temp: 37 °C
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 15 g/dl of total protein.
If the obtained results are greater than 15 g/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HB020
Total protein in Urine and CSF
VOL 2 x 125 ml
Colorimetric test. Pyrogallol Red
Standard 1 x 5 mL
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard
Standard 20 µl
Sample 20 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 10 minutes at 15-25°C or 5 min at 37°C. After the incubation
time, aspirate and measure all the samples within 30 min after preparation.
PROGRAM SETUP
Num of Blank: 3
3
These values are for urine samples. For CSF samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 4000 mg/l of TPU.
If the obtained results are greater than 4000 mg/l, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HB021
Triglycerides
VOL 12 x 20 ml
Enzymatic-colorimetric test.
Standard 1 x 5 mL GPO-POD
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
Standard1 10 µl
Sample 10 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 10 minutes at 15-25°C or 5 min at 37°C. After the incubation
time, aspirate and measure all the samples within 30 min after preparation.
PROGRAM SETUP
Program Name: TRIG Blank Low: 0.00002
Program Method: End Point Blank High: 0.14002
Main Filter: 510 Normal Low: 35.0000 mg/dL
Sub Filter: None Normal High: 160.0000 mg/dL
Program Unit: mg/dL Num of STD: 1
Aspiration Volume: 0500 µl CONC: 200.00001 mg/dL
Delay Time: 001 sec Factor: 0.0000
Test Time: 003 sec Control N Min: 0.00004 mg/dL
Dilution Factor: 1.0000 Control N Max: 0.00004 mg/dL
4
Linearity Min: 0.0000 mg/dL Control P Min: 0.0000 mg/dL
Linearity Max: 1200.0000 mg/dL Control P Max: 0.00004 mg/dL
Blank: Reagent Cuvette Temp: 37 °C
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 1200 mg/dl of Triglycerides.
If the obtained results are greater than 1200 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and
multiply the result by factor 2.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
Standard1 10 µl
Sample 10 µl
Reagent 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 10 minutes at 15-25°C or 5 min at 37°C. After the incubation
time, aspirate and measure all the samples within 30 min after preparation.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 1000 mg/dl of Triglycerides.
If the obtained results are greater than 1000 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and
multiply the result by factor 2.
All the components of the kit are stable at 2-8°C up to the date of expiration as specified, when stored tightly closed, protected
from light and contaminations prevented during their use.
The reagent should be discarded if turbidity or precipitation has occurred or if the blank absorbance is out of range2. Handle
standard very carefully to prevent contamination.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
1
Standard 10 µl
Sample 10 µl
Working solution (R1+R3) 1.0 ml 1.0 ml 1.0 ml
Mix and incubate for 10 min at 15-25°C or 5 min at 37°C. And then add:
Reagent 2 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 10 min at 15-25°C or 5 min at 37°C. After the incubation
time, aspirate and measure all the samples within 30 min after addition of the reagent 2.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
3
These values are for serum or plasma samples. For urine samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 225 mg/dl of urea.
If the obtained results are greater than 225 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
REF HBL03
Urea Liquid
VOL 160 + 40 ml
U.V. Kinetic test
Standard 1 x 5 ml Urease-GLDH
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Pre-rinse Standard1 Sample
1
Standard 20 µl 10 µl
Sample 10 µl
Working solution (R1+R2) 1.0 ml 2.0 ml 1.0 ml 1.0 ml
Before calibration, rinse the CYANSmart with the Pre-rinse mixture after 2 min incubation at 37°C using the “Wash” button.*
Prepare, mix and measure one sample at a time. Aspirate the mixture in the CYANSmart, immediately after addition of the
working solution to the sample/(calibrator). Wait with the preparation of the next sample until the CYANSmart is finished with
measuring the previous one. At this time, the CYANSmart will asks: “Press PUSH Aspirate Sample”. **
PROGRAM SETUP
Program Name: UREAL Blank Low: 1.0000²
Program Method: Two Point Blank High: 2.5000²
Main Filter: 340 Normal Low: 15.0000³ mg/dL
Sub Filter: None Normal High: 45.0000³ mg/dL
Program Unit: mg/dL Num of STD: 1
Aspiration Volume: 0800 µl CONC: 50.00001 mg/dL
Delay Time: 030 sec Factor: 0.0000
Test Time: 060 sec Control N Min: 0.00004 mg/dL
Dilution Factor: 1.0000 Control N Max: 0.00004 mg/dL
4
Linearity Min: 0.74300 mg/dL Control P Min: 0.0000 mg/dL
Linearity Max: 400.0000 mg/dL Control P Max: 0.00004 mg/dL
Blank: Reagent² Cuvette Temp: 37 °C
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned on the insert
provided with HBC03.
² Programming reagent as blank gives you the advantage that deterioration of the reagent can be easily detected. Alternatively, you can program
and aspirate distilled water as blank, with values for Blank Low: 0.0000 and Blank High: 0.0100.
3
These values are for serum or plasma samples. For urine samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 400 mg/dl of urea. If the obtained results are greater than 400 mg/dl, dilute the sample 1:2 with saline
solution, repeat the determination, and multiply the result by factor 2.
NOTES
*
Prerinsing the CYANSmart flowcell with the Pre-rinse mixture is essential to improve the calibration accuracy.
**
Carry-over by pathological samples is possible. To prevent this, we recommend to follow a sample with concentration >50 mg/dl
by aspiration of 0.8 ml Reagent Blank (working solution) before proceeding with the next sample.
SAMPLE PREPARATION
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
Standard1 25 µl
Sample 25 µl
Working solution (R1+R2) 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 10 min at 15-25°C or 5 min at 37°C. After the incubation
time, aspirate and measure all the samples within 30 min after addition of the working reagent.
PROGRAM SETUP
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
3
These values are for serum or plasma samples. For urine samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 40 mg/dl of uric acid.
If the obtained results are greater than 40 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
SAMPLE PREPARATION
Use the standard included in the kit1.
Make sure the reagents and samples are at room temperature.
Then, pipette into a test tube:
Blank Sample Standard1
Standard1 25 µl
Sample 25 µl
Working solution (R1+R2) 1.0 ml 1.0 ml 1.0 ml
You can prepare several samples simultaneously. Mix and incubate for 10 min at 15-25°C or 5 minutes at 37°C. After the incubation
time, aspirate and measure all the samples within 45 min after addition of the working reagent.
PROGRAM SETUP
Program Name: UAL Blank Low: 0.00002
Program Method: End Point Blank High: 0.12002
Main Filter: 510 Normal Low: 2.5000³ mg/dL
Sub Filter: None Normal High: 7.7000³ mg/dL
Program Unit: mg/dL Num of STD: 1
Aspiration Volume: 0500 µl CONC: 6.00001 mg/dL
Delay Time: 001 sec Factor: 0.0000
Test Time: 003 sec Control N Min: 0.00004 mg/dL
Dilution Factor: 1.0000 Control N Max: 0.00004 mg/dL
4
Linearity Min: 0.0600 mg/dL Control P Min: 0.0000 mg/dL
Linearity Max: 25.0000 mg/dL Control P Max: 0.00004 mg/dL
Blank: Reagent Cuvette Temp: 37 °C
Num of Blank: 1
1
Alternatively, you can use the Biochemistry Calibrator (HBC03) for calibration. Program NUM of STD: 1 and CONC: as mentioned
on the insert provided with HBC03.
3
These values are for serum or plasma samples. For urine samples; please check the insert for the values and sample preparation.
4
The control values can be found on the control sheets delivered together with the control
LINEARITY
This method is linear up to 25 mg/dl of uric acid.
If the obtained results are greater than 25 mg/dl, dilute the sample 1:2 with saline solution, repeat the determination, and multiply
the result by factor 2.
LIN340
Once every year, CYANSmart should be validated to assure correct results.
PROGRAM SETUP
LIN510
Once every year, CYANSmart should be validated to assure correct results.
PROGRAM SETUP
English
To all Healthcare Professionals,
CYANSmart
Cypress Diagnostics provides the tools and solutions that
let clinical laboratories worldwide deliver clear and precise
diagnostic results.
We manufacture the equipment needed for handling the
Semi-Automatic Biochemistry
samples, analyzers to perform the tests, reagents to carry out
the tests and - increasingly often - the software platforms to
report the results.
Kind regards,
ISO 13485-2016
www.diagnostics.be • Belgium • Tel: ++ 32 15 67 67 68 • e-mail: cypress@diagnostics.be
CYANSmart Technical Specifications