HIV I&II Rapid Test
Rapid HCG Pregnancy Test Card
Intended Use
HCG Pregnancy Urine Test is a chromatographic immunoassay for the early detection of human chrionic gonadotropin (HCG) in urine specimens.
Contents of Kit
HCG Pregnancy Test Card 25 ea
Instructions For Use 1 ea
Storage And Stability
The kits should be stored at temperature 4-30ípC in the sealed pouch for the duration of the shelf life.
Pre Cautions
1. For in vitro diagnostic use only.
2. Do not use after expiration date.
3. Test device should remain sealed until use.
25 tests/kit, 40 kits/carton
Rapid Influenza A + B Test Card
Intended Use
Influenza A+B Test is an in vitro immunochromatographic assay for the qualitative detection of influenza type A and type B nucleoprotein antigens in nasopharyngeal swab, nasal swab and nasal aspirate samples. The identification is based on the monoclonal antibodies specific for the nucleoprotein of Influenza virus A. It is intended to aid in the rapid diagnosis of influenza infection. Negative results should be confirmed by other methods, such as cell culture.
Contents of Kit
Flu A + B Test Card 20 ea
Sample Extraction Buffer 1 ea
Extraction Tube 20 ea
Nozzle With Filter 21 ea
Sterilized Swab 20 ea
Tube Stand 1 ea
Instructions For Use 1 ea
Storage And Stability
Store the Influenza A+B Rapid Test at room temperature or refrigerated (2-30ípC). Do not freeze. All reagents are stable until the expiration dates marked on their outer packaging and buffer vial.
Pre Cautions
1. For in vitro diagnostic use only.
2. Do not use after the expiration date.
3. The test device should remain in the sealed pouch until use.
4. If the Influenza A+B Rapid Test kit was kept refrigerated, let all the reagents warm up to room temperature (15ípC -30ípC) before proceeding with the test.
5. Wear gloves when handing the samples, avoid touching the reagent membrane with your fingers.
6. Discard gloves, swabs, test tubes, and test devices in accordance with the local regulation.
7. Visibly bloody samples should not be used for the testing.
25 tests/kit, 40 kits/carton
Rapid Malaria pf/pv Antigen Test Card
Intended Use
Malaria pf (HRP II) / pv (LDH) Antigen Test is for the rapid qualitative determination of Malaria P. falciparum specific histidine rich protein-2 (Pf HRP-2) and Malaria P. vivax specific lactate dehydrogenase (pvLDH) in human blood as an aid in the diagnosis of Malaria infection.
Contents of Kit
Malaria pf/pv Antigen Test Card 25 ea
Malaria Sample Buffer 1 ea
Instructions For Use 1 ea
Storage And Stability
The kit can be stored at room temperature or refrigerated (4-30ípC). The test device is stable through the expiration date printed on the sealed pouch. The test device must remain in the sealed pouch until use. DO NOT FREEZE. Do not use beyond the expiration date.
Pre Cautions
1. For professional in vitro diagnostic use only. Do not use after expiration date.
2. Do not eat, drink or smoke in the area where the specimens or kits are handled.
3. Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout testing and follow the standard procedures for proper disposal of specimens.
4. Wear protective clothing such as laboratory coats, disposable gloves and eye protection when specimens are being tested.
5. Humidity and temperature can adversely affect results.
25 tests/kit, 40 kits/carton
