| Certification: | MSDS, ISO13485 |
|---|---|
| Group: | Female |
| Component: | Rapid Test + Buffer + Pipettes |
| Specimen: | Whole Blood, Serum, Plasma |
| Storage: | 2~30 º C |
| Principle: | Lateral Flow Chromatographic Immunoassay |
| Samples: |
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| Customization: |
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Audited Supplier INTENDED USE
Rubella IgG/IgM Rapid test is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to Rubella virus in human serum or plasma. This test provides only a preliminary test result. Therefore, more specific alternative diagnosis method such as Sabin-Feldman dye test for IgG antibodies, the IgM-IFA (Immuno-fluorescent Antibody) test and the PCR test must be used in order to obtain a confirmation of Rubella infection.
| Storage | 2~30 º C |
| Specimen | Whole Blood/Serum/Plasma |
| Component | Rapid Test + Buffer + Pipettes |
| Principle | Colloidal gold rapid tests |
| Reading | Within 15mins |
| Package | 40tests/box |
| Trademark | Dewei |
| Origin | China |
INTRODUCTION
Rubella (commonly known as German measles or 3-day measles) is an infection that primarily affects the skin and lymph nodes. It is caused by the rubella virus (not the same virus that causes measles), which is usually transmitted by secretions from the nose or throat. It can also pass through a pregnant woman's bloodstream to infect her unborn child. As this is a generally mild disease in children, the primary medical danger of rubella is the infection of pregnant woman, which may cause congenital rubella syndrome in developing babies.
MAIN CONTENTS
• A reaction test Cassette with desiccant.
• Buffer
• Disposable pipettes.
• Instructions for use.
STORAGE AND STABILITY
• Store at 2 ~ 30 º C in the sealed pouch for 24 months.
PRECAUTIONS
• For in vitro diagnostic use only.
• Do not use after expiration date.
• The test Cassette should remain in the sealed pouch until use.
• The used test Cassette should be discarded according to local regulations.
DIRECTION OF USE
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EXHIBITIONS
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