Comparison |
| CLIA Classification |
CLIA Waived | CLIA Waived for Whole Blood / CLIA Moderately Complex for Serum, Plasma | CLIA Waived | CLIA Waived for Whole Blood | CLIA Waived for Whole Blood / CLIA Moderate Complexity for Serum, Plasma |
| CLIA Classified |
CLIA Waived | CLIA Waived Sample Dependent | CLIA Waived | CLIA Waived Sample Dependent | CLIA Waived Sample Dependent |
| Contents 1 |
- Single Use Test Devices
- Buffered Developer Solution Vials
- Test Stands
- Specimen Collection Loops
- Package Insert
| (25) Cassettes in Sealed Pouches, (25) 10 µL Black Line Sample Transfer Pipettes for use with Serum / Plasma, (25) 25 µL Red Line Sample Transfer Pipettes for use with Whole Blood, 6 mL Developer Solution, 0.5 mL Negative Control, 0.5 mL Positive Control, Instructional insert, Procedure card | (10) Individually Packaged Sample Collector, (10) Individually Packaged Test Cassette, (10) Buffer Vial, Package Insert | (25) Test Sticks, (25) Test Tubes, (25) Capillary Tubes with Capillary Bulb, Positive Control, Negative Control, Developer Buffer, (25) Transfer Pipets, Workstation | (25) Test Sticks in Container, (25) Test Tubes, (25) Transfer Pipettes, Diluent, Mono Positive Control, Mono Negative Control, Workstation, Directional Insert |
| Is_ECAT |
| | N | | |
| Is_GSA |
| | Y | | |
| Is_VA |
| | N | | |
| Latex Free Indicator |
| Not Made with Natural Rubber Latex | | | |
| Number of Tests |
100 Tests | 25 Tests | 10 Tests | 25 Tests | 25 Tests |
| Product Dating |
McKesson Acceptable Dating: we will ship >= 180 days | McKesson Acceptable Dating: we will ship >= 90 days | McKesson Acceptable Dating: we will ship >= 90 days | McKesson Acceptable Dating: we will ship >= 90 days | McKesson Acceptable Dating: we will ship >= 90 days |
| Sample Type |
Whole Blood Sample | Whole Blood / Serum / Plasma Sample | Tear Sample | Whole Blood / Serum / Plasma Sample | Whole Blood / Serum / Plasma Sample |
| Technology |
| | Direct Sampling Micro-Filtration Technology | | Immunochromatographic Dipstick Technology |
| Test Format |
Test Device Format | Cassette Format | Cassette Format | Test Strip Format | Test Strip Format |
| Test Method |
Lateral Flow Method | | Lateral Flow Method | | Chromatographic Immunoassay |
| Test Name |
Hepatitis C Test | Infectious Mononucleosis | Acute Conjunctivitis (Pink Eye) | Infectious Mononucleosis | Infectious Mononucleosis |
| Test Type |
Antibody Test | Infectious Disease Immunoassay | Infectious Disease Immunoassay | Infectious Disease Immunoassay | Infectious Disease Immunoassay |
| Time to Results |
20 Minute Results | 8 Minute Results | 10 Minute Results | 5 Minute Results | 5 Minute Results |
| UNSPSC Code |
41116126 | 41116126 | 41116144 | 41116126 | 41116126 |
| Application |
Other Infectious Disease Test Kit | Other Infectious Disease Test Kit | Other Infectious Disease Test Kit | Other Infectious Disease Test Kit | Other Infectious Disease Test Kit |
| Country of Origin |
United States | United States | United States | United States | United States |
| Purchase Program Type |
Standard Purchase | Standard Purchase | Standard Purchase | Standard Purchase | Standard Purchase |
| Reading Type |
Visual Read | Visual Read | Visual Read | Visual Read | Visual Read |
| Specialty |
Immunoassay | Immunoassay | Immunoassay | Immunoassay | Immunoassay |
| Test Kit Type |
Rapid | Rapid | Rapid | Rapid | Rapid |
| Features and Benefits |
- The OraQuick® HCV test is FDA approved for detecting HCV antibodies in fingerstick and venipuncture whole blood
- Our simple platform enables healthcare providers to deliver an accurate diagnosis in 20 minutes
- The OraQuick HCV Rapid Antibody Test is comprised of both a single-use test device and vial containing a pre-measured amount of a buffered developer solution
- The test consists of a sealed pouch with two separate compartments for each component
- The developer solution facilitates the capillary flow of the specimen into the device and onto the assay strip
- Kit includes: 100 divided pouches each containing a test device, absorbent packet, and developer solution vial (each contains 0.75 mL of a buffered saline solution with an antimicrobial agent); 10 reusable test stands; 100 specimen collection loops; package insert
|
- McKesson Consult™ Mononucleosis Cassette Test
- A rapid test for the qualitative detection of Infectious Mononucleosis (IM) heterophile antibodies in whole blood, serum and plasma.
- CLIA Waived for Whole Blood / CLIA Moderately Complex for Serum or Plasma.
- Contents: 25 Cassettes (in sealed pouches), 25 (10 µL) (black line) Sample transfer pipettes for use with serum/plasma, 25 (25 µL) (red line) Sample transfer pipettes for use with whole blood, Developer solution (6 mL; Phosphate saline buffer containing 0.1% Sodium Azide as a preservative), Negative control (0.5 mL; diluted human serum containing 0.1% Sodium Azide as a preservative), Positive control (0.5 mL; diluted human serum containing IM Heterophile Antibodies and 0.1% Sodium Azide as a preservative), Instructional insert, Procedure card
- Results in as fast as eight minutes.
- Greater than 99% accuracy.
- External positive and negative quality controls provided.
- Acute infection determination (IgM Specific Conjugate).
- For in vitro diagnostic use only.
- 18-month shelf life.
- Not made with natural rubber latex.
- Packaged: 25 Tests Per Box
|
- QuickVue Adenoviral conjunctivitis Test is a CLIA-waived test for the visual, qualitative in vitro detection of Adenoviral antigens (hexon protein) directly from eye fluid
- Identify, isolate and manage contagious patients, preventing spread to other patients and staff
- Offers an accurate, fast, disposable platform that is easy to use
- 90% sensitivity and 96% specificity
- Disposable test
- No additional equipment is needed to administer or interpret
|
- A simple, rapid test for the detection of heterophile antibodies specific to Infectious Mononucleosis (IM).
- Provides highly accurate results in 5 minutes
- CLIA Waived for whole blood; CLIA Non-Waived for Serum or Plasma
|
- 99% sensitivity; 96% specificity
- Results in 5 minutes
- 99% sensitivity; 96% specificity
- Kit includes positive and negative controls
|
