CLARITY ONE-STEP IMMUNO FECAL OCCULT BLOOD TEST KIT
No Food, Vitamin, or Iron Restrictions
0.05ug hHB/ml Monoclonal Antibody
Built-in QC
Room Temperature Storage
Contains External Controls (DTG-FOBCTLS)
28 Month Dating
CLIA Waived
Contains: 30-IFOB Test Cassettes, 35-Sample Collection Buffer Tubes, 1-Positive Control, 1-Negative Control, and Package Insert
Manufacturer
Clarity Diagnostic
Number Of Tests
30 Tests
Sold By
Box of 30
Test Type
Colorectal Cancer Screening
Time to Results
5 minutes
How reliable is the immunochemical method used in this iFOB test compared to other available methods?
The immunochemical method in the iFOB test, using a monoclonal antibody, is designed to be highly specific, reducing the likelihood of false positives compared to older guaiac-based fecal occult blood tests [Manufacturer Info].
Since there are no dietary restrictions, can patients be confident in the results even after consuming foods typically avoided before such tests?
Yes, patients can be confident in the results as the Clarity iFOB test does not require dietary restrictions, thereby minimizing the risk of diet-related false positives [Manufacturer Info].
Could you walk me through the steps of conducting the test, particularly if I'm using it in a high-paced clinic environment?
To conduct the test, collect a fecal sample using the buffer tube, apply the sample to the cassette, wait 5 minutes for results, and then compare the results with the built-in quality control [Manufacturer Info].
In the case that the test result is positive, what immediate actions should a healthcare provider take?
If the test result is positive, the healthcare provider should recommend follow-up diagnostic procedures such as a colonoscopy to confirm the presence of gastrointestinal bleeding or other conditions [Manufacturer Info].
How does the built-in quality control feature enhance the accuracy of the test results?
The built-in quality control in the iFOB test ensures the test is working correctly each time it is used, enhancing reliability and accuracy of the results [Manufacturer Info].
Are there any storage instructions that need to be strictly followed, especially in varying temperature settings?
The Clarity iFOB test should be stored at room temperature, ensuring that it is kept away from extreme temperatures to maintain its efficacy [Product Specs].
What should I do if I encounter a discrepancy between the external controls and the test results?
If there is a discrepancy between external controls and test results, retest with a new cassette and consider reviewing the storage and handling procedures to ensure they meet guidelines [Manufacturer Info].
Can you explain how the CLIA waiver status impacts who is able to perform this test, particularly in smaller clinical settings?
The CLIA waiver status allows non-laboratory trained personnel to perform the test in various settings, including smaller clinics, increasing accessibility and convenience [Industry Standards].
Considering the 5-minute result time, how does this speed influence workflow efficiency in a busy practice?
The 5-minute result time allows for quick clinical decisions, significantly enhancing workflow efficiency and patient throughput in busy medical practices [Product Specs].
CLARITY ONE-STEP IMMUNO FECAL OCCULT BLOOD TEST KIT
No Food, Vitamin, or Iron Restrictions
0.05ug hHB/ml Monoclonal Antibody
Built-in QC
Room Temperature Storage
Contains External Controls (DTG-FOBCTLS)
28 Month Dating
CLIA Waived
Contains: 30-IFOB Test Cassettes, 35-Sample Collection Buffer Tubes, 1-Positive Control, 1-Negative Control, and Package Insert
Manufacturer
Clarity Diagnostic
Number Of Tests
30 Tests
Sold By
Box of 30
Test Type
Colorectal Cancer Screening
Time to Results
5 minutes
How reliable is the immunochemical method used in this iFOB test compared to other available methods?
The immunochemical method in the iFOB test, using a monoclonal antibody, is designed to be highly specific, reducing the likelihood of false positives compared to older guaiac-based fecal occult blood tests [Manufacturer Info].
Since there are no dietary restrictions, can patients be confident in the results even after consuming foods typically avoided before such tests?
Yes, patients can be confident in the results as the Clarity iFOB test does not require dietary restrictions, thereby minimizing the risk of diet-related false positives [Manufacturer Info].
Could you walk me through the steps of conducting the test, particularly if I'm using it in a high-paced clinic environment?
To conduct the test, collect a fecal sample using the buffer tube, apply the sample to the cassette, wait 5 minutes for results, and then compare the results with the built-in quality control [Manufacturer Info].
In the case that the test result is positive, what immediate actions should a healthcare provider take?
If the test result is positive, the healthcare provider should recommend follow-up diagnostic procedures such as a colonoscopy to confirm the presence of gastrointestinal bleeding or other conditions [Manufacturer Info].
How does the built-in quality control feature enhance the accuracy of the test results?
The built-in quality control in the iFOB test ensures the test is working correctly each time it is used, enhancing reliability and accuracy of the results [Manufacturer Info].
Are there any storage instructions that need to be strictly followed, especially in varying temperature settings?
The Clarity iFOB test should be stored at room temperature, ensuring that it is kept away from extreme temperatures to maintain its efficacy [Product Specs].
What should I do if I encounter a discrepancy between the external controls and the test results?
If there is a discrepancy between external controls and test results, retest with a new cassette and consider reviewing the storage and handling procedures to ensure they meet guidelines [Manufacturer Info].
Can you explain how the CLIA waiver status impacts who is able to perform this test, particularly in smaller clinical settings?
The CLIA waiver status allows non-laboratory trained personnel to perform the test in various settings, including smaller clinics, increasing accessibility and convenience [Industry Standards].
Considering the 5-minute result time, how does this speed influence workflow efficiency in a busy practice?
The 5-minute result time allows for quick clinical decisions, significantly enhancing workflow efficiency and patient throughput in busy medical practices [Product Specs].
CLARITY ONE-STEP IMMUNO FECAL OCCULT BLOOD TEST KIT
No Food, Vitamin, or Iron Restrictions
0.05ug hHB/ml Monoclonal Antibody
Built-in QC
Room Temperature Storage
Contains External Controls (DTG-FOBCTLS)
28 Month Dating
CLIA Waived
Contains: 30-IFOB Test Cassettes, 35-Sample Collection Buffer Tubes, 1-Positive Control, 1-Negative Control, and Package Insert
Manufacturer
Clarity Diagnostic
Number Of Tests
30 Tests
Sold By
Box of 30
Test Type
Colorectal Cancer Screening
Time to Results
5 minutes
How reliable is the immunochemical method used in this iFOB test compared to other available methods?
The immunochemical method in the iFOB test, using a monoclonal antibody, is designed to be highly specific, reducing the likelihood of false positives compared to older guaiac-based fecal occult blood tests [Manufacturer Info].
Since there are no dietary restrictions, can patients be confident in the results even after consuming foods typically avoided before such tests?
Yes, patients can be confident in the results as the Clarity iFOB test does not require dietary restrictions, thereby minimizing the risk of diet-related false positives [Manufacturer Info].
Could you walk me through the steps of conducting the test, particularly if I'm using it in a high-paced clinic environment?
To conduct the test, collect a fecal sample using the buffer tube, apply the sample to the cassette, wait 5 minutes for results, and then compare the results with the built-in quality control [Manufacturer Info].
In the case that the test result is positive, what immediate actions should a healthcare provider take?
If the test result is positive, the healthcare provider should recommend follow-up diagnostic procedures such as a colonoscopy to confirm the presence of gastrointestinal bleeding or other conditions [Manufacturer Info].
How does the built-in quality control feature enhance the accuracy of the test results?
The built-in quality control in the iFOB test ensures the test is working correctly each time it is used, enhancing reliability and accuracy of the results [Manufacturer Info].
Are there any storage instructions that need to be strictly followed, especially in varying temperature settings?
The Clarity iFOB test should be stored at room temperature, ensuring that it is kept away from extreme temperatures to maintain its efficacy [Product Specs].
What should I do if I encounter a discrepancy between the external controls and the test results?
If there is a discrepancy between external controls and test results, retest with a new cassette and consider reviewing the storage and handling procedures to ensure they meet guidelines [Manufacturer Info].
Can you explain how the CLIA waiver status impacts who is able to perform this test, particularly in smaller clinical settings?
The CLIA waiver status allows non-laboratory trained personnel to perform the test in various settings, including smaller clinics, increasing accessibility and convenience [Industry Standards].
Considering the 5-minute result time, how does this speed influence workflow efficiency in a busy practice?
The 5-minute result time allows for quick clinical decisions, significantly enhancing workflow efficiency and patient throughput in busy medical practices [Product Specs].
CLARITY ONE-STEP IMMUNO FECAL OCCULT BLOOD TEST KIT
No Food, Vitamin, or Iron Restrictions
0.05ug hHB/ml Monoclonal Antibody
Built-in QC
Room Temperature Storage
Contains External Controls (DTG-FOBCTLS)
28 Month Dating
CLIA Waived
Contains: 30-IFOB Test Cassettes, 35-Sample Collection Buffer Tubes, 1-Positive Control, 1-Negative Control, and Package Insert
Manufacturer
Clarity Diagnostic
Number Of Tests
30 Tests
Sold By
Box of 30
Test Type
Colorectal Cancer Screening
Time to Results
5 minutes
How reliable is the immunochemical method used in this iFOB test compared to other available methods?
The immunochemical method in the iFOB test, using a monoclonal antibody, is designed to be highly specific, reducing the likelihood of false positives compared to older guaiac-based fecal occult blood tests [Manufacturer Info].
Since there are no dietary restrictions, can patients be confident in the results even after consuming foods typically avoided before such tests?
Yes, patients can be confident in the results as the Clarity iFOB test does not require dietary restrictions, thereby minimizing the risk of diet-related false positives [Manufacturer Info].
Could you walk me through the steps of conducting the test, particularly if I'm using it in a high-paced clinic environment?
To conduct the test, collect a fecal sample using the buffer tube, apply the sample to the cassette, wait 5 minutes for results, and then compare the results with the built-in quality control [Manufacturer Info].
In the case that the test result is positive, what immediate actions should a healthcare provider take?
If the test result is positive, the healthcare provider should recommend follow-up diagnostic procedures such as a colonoscopy to confirm the presence of gastrointestinal bleeding or other conditions [Manufacturer Info].
How does the built-in quality control feature enhance the accuracy of the test results?
The built-in quality control in the iFOB test ensures the test is working correctly each time it is used, enhancing reliability and accuracy of the results [Manufacturer Info].
Are there any storage instructions that need to be strictly followed, especially in varying temperature settings?
The Clarity iFOB test should be stored at room temperature, ensuring that it is kept away from extreme temperatures to maintain its efficacy [Product Specs].
What should I do if I encounter a discrepancy between the external controls and the test results?
If there is a discrepancy between external controls and test results, retest with a new cassette and consider reviewing the storage and handling procedures to ensure they meet guidelines [Manufacturer Info].
Can you explain how the CLIA waiver status impacts who is able to perform this test, particularly in smaller clinical settings?
The CLIA waiver status allows non-laboratory trained personnel to perform the test in various settings, including smaller clinics, increasing accessibility and convenience [Industry Standards].
Considering the 5-minute result time, how does this speed influence workflow efficiency in a busy practice?
The 5-minute result time allows for quick clinical decisions, significantly enhancing workflow efficiency and patient throughput in busy medical practices [Product Specs].
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