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Blood Infectious disease screening test 4 in 1 combo test kit of HBsAg HIV HCV Syphilis rapid test
Blood Infectious disease screening test 4 in 1 combo test kit of HBsAg HIV HCV Syphilis rapid test
Blood Infectious disease screening test 4 in 1 combo test kit of HBsAg HIV HCV Syphilis rapid test
Blood Infectious disease screening test 4 in 1 combo test kit of HBsAg HIV HCV Syphilis rapid test
Blood Infectious disease screening test 4 in 1 combo test kit of HBsAg HIV HCV Syphilis rapid test
Blood Infectious disease screening test 4 in 1 combo test kit of HBsAg HIV HCV Syphilis rapid test
Blood Infectious disease screening test 4 in 1 combo test kit of HBsAg HIV HCV Syphilis rapid test
Blood Infectious disease screening test 4 in 1 combo test kit of HBsAg HIV HCV Syphilis rapid test

Blood Infectious disease screening test 4 in 1 combo test kit of HBsAg HIV HCV Syphilis rapid test

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Quick Details

Brand Name:
MR
Model Number:
HIV/HBSAG/HCV
Quality Certification:
ISO13485
Safety standard:
MSDS
Product name:
HIV/HBSAG/HCV
Format:
Strip/cassette
Dimension:
3.0mm/4.0mm
Specimen:
Whole blood/serum/plasma
Package:
25 pcs/box;50pcs/box
Storage:
4-30°C
Method:
Immunochromatography
MOQ:
1000pcs
Brand:
MR

Quick Details

Warranty:
2 years
After-sale Service:
Online technical support
Place of Origin:
Shandong, China
Brand Name:
MR
Model Number:
HIV/HBSAG/HCV
Quality Certification:
ISO13485
Safety standard:
MSDS
Product name:
HIV/HBSAG/HCV
Format:
Strip/cassette
Dimension:
3.0mm/4.0mm
Specimen:
Whole blood/serum/plasma
Package:
25 pcs/box;50pcs/box
Storage:
4-30°C
Method:
Immunochromatography
MOQ:
1000pcs
Brand:
MR
Product Description
Specification
item
value
Place of Origin
China
Shandong
Brand Name
MR
Model Number
HIV
Power Source
Manual
Warranty
2 years
After-sale Service
Online technical support
Material
plastic, paper
Shelf Life
2 years
Quality Certification
ISO13485
Instrument classification
Class II
Safety standard
MSDS
Product name
HIV/HBSAG/HCV rapid test
Format
Strip/Triple line cassette
Dimension
3.0mm/4.0mm
Specimen
Whole blood/serum/plasma
Package
25 pcs/box;50pcs/box
Storage
4-30°C
Shelf Life
24months
Method
Immunochromatography
MOQ
1000pcs
Brand
MR

Intended Use

The reagent is used to detect the Hepatitis C Virus Antibody in serum/plasma/whole blood qualitatively.

Test procedure

1. Instruction for Use must be read entirely before taking the test. Allow the test device controls to equilibrate to room
temperature for 30 minutes (20°C-30°C) prior to testing. Do not open the inner packaging until ready, it must be used in one hour if opened.
2. 2. Test Procedure
Strip:
(1) Remove the test strip from the sealed pouch, place it on a clean and level surface with the sample adding area up.
(2) Using the dropper, vertically transfer one(1) drop (25µl) of serum/plasma/whole blood sample onto the sample adding area of the strip, avoiding the formation of bubbles. Add two(2) drops (80-100ul) of sample buffer onto the sample adding area of the strip.
(3) Observe the test results immediately within 10-20 minutes, the result is invalid over 20 minutes.
Cassette:
* (1) Remove the test cassette from the sealed pouch, place it on a clean and level surface with the sample well up.
* (2) Using the dropper, vertically transfer one(1) drop (25µl) of serum/plasma/whole blood sample into the sample well (S) of the cassette, avoiding the formation of bubbles. Add two(2) drops (80-100ul) of sample buffer into the sample well of the cassette.
(3) Observe the test results immediately within 10-20 minutes, the result is invalid over 20 minutes.
* Don't read result after 20 minutes. To avoid confusion, discard the test device after interpreting the result.
Result Judgment
POSITIVE : Two (2) distinct colored lines appear. One line should be in the control region (C) and the other line should be in the test region (T).
NEGATIVE : One (1) colored line appears in the control region(C). No apparent colored line appears in the test region (T).The negative result does not indicate the absence of analytes in the sample, it only indicates the level of tested analytes in the sample is less than cut-off level.
INVALID : No colored lines appear or control line fails to appear, indicating that the operator error or reagent failure. Verify the test procedure and repeat the test with a new testing device.
Manufacturing procedure
Packing & Delivery
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