In 3 easy steps Multiplo HbB/HBC/HIV instantly detects antibodies to all three viruses in whole blood, serum or plasma. The quality and performance of this test is second to none with a sensitivity of 99.1%.
Multiplo Hep B/C/HIV is a rapid, flow-through diagnostic immunoassay developed to utilize the performance characteristics of a conventional diagnostic immunoassay while simplifying the test procedure to eliminate the requirement for expensive equipment and highly trained personnel and decrease turnaround time.
Methodology:
Rapid Vertical Flow Immunoassay. Manually performed, visually interpreted
Test Principle:
Multiplo Rapid HBc/HIV/HCV Antibody Test (Multiplo HBc/HIV/HCV) is a qualitative rapid vertical flow test to detect the presence of antibodies to human immunodeficiency virus (HIV) type 1 and 2 (HIV-1/2), hepatitis B virus core antigen (HBc), and hepatitis C virus (HCV) in human serum, plasma or whole blood specimens.
Sample Size: 1 drop
Sample Type: blood, serum, or plasma
Operating range: 2-30°C or 35-85°F
Shelf Life: 24 month shelf-life at 2 – 30° C
Controls: External test controls available as an accessory
Sensitivity: 99.1% in serum
Specificity: 98.6% in serum
(Fingerstick Whole Blood) Includes a test tray in each pouch
1 test cartridge
1 instant/gold cap
1 silica gel packet
1 auto-fill pipette
1 sample tube
1 Universal Buffer
1 lancet (sterile)
1 alcohol swab
1 package insert
There are three formats:
Point-of-Care:
This format includes a test tray in each pouch and is ideally suited to testing at the point of patient care, settings such as mobile clinics requiring a portable and all-in-one testing solution.
Cat. No. 815311004551
Qty. 20 tests per box
LAB+:
This format maximizes customer flexibility in for testing serum, plasma, and whole blood specimens.
Cat. No.815311004575
Qty. 50 tests per box
LAB S/P:
This format is ideally suited for laboratories using serum and plasma specimens, and batch testing.
Cat. No. 815311004582
Qty. 50 tests per box
Manufactured in Canada by MedMira in an ISO 13485 certified facility
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In 3 easy steps Multiplo HbB/HBC/HIV instantly detects antibodies to all three viruses in whole blood, serum or plasma. The quality and performance of this test is second to none with a sensitivity of 99.1%.
Multiplo Hep B/C/HIV is a rapid, flow-through diagnostic immunoassay developed to utilize the performance characteristics of a conventional diagnostic immunoassay while simplifying the test procedure to eliminate the requirement for expensive equipment and highly trained personnel and decrease turnaround time.
Methodology:
Rapid Vertical Flow Immunoassay. Manually performed, visually interpreted
Test Principle:
Multiplo Rapid HBc/HIV/HCV Antibody Test (Multiplo HBc/HIV/HCV) is a qualitative rapid vertical flow test to detect the presence of antibodies to human immunodeficiency virus (HIV) type 1 and 2 (HIV-1/2), hepatitis B virus core antigen (HBc), and hepatitis C virus (HCV) in human serum, plasma or whole blood specimens.
Sample Size: 1 drop
Sample Type: blood, serum, or plasma
Operating range: 2-30°C or 35-85°F
Shelf Life: 24 month shelf-life at 2 – 30° C
Controls: External test controls available as an accessory
Sensitivity: 99.1% in serum
Specificity: 98.6% in serum
(Fingerstick Whole Blood) Includes a test tray in each pouch
1 test cartridge
1 instant/gold cap
1 silica gel packet
1 auto-fill pipette
1 sample tube
1 Universal Buffer
1 lancet (sterile)
1 alcohol swab
1 package insert
There are three formats:
Point-of-Care:
This format includes a test tray in each pouch and is ideally suited to testing at the point of patient care, settings such as mobile clinics requiring a portable and all-in-one testing solution.
Cat. No. 815311004551
Qty. 20 tests per box
LAB+:
This format maximizes customer flexibility in for testing serum, plasma, and whole blood specimens.
Cat. No.815311004575
Qty. 50 tests per box
LAB S/P:
This format is ideally suited for laboratories using serum and plasma specimens, and batch testing.
Cat. No. 815311004582
Qty. 50 tests per box
Manufactured in Canada by MedMira in an ISO 13485 certified facility