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Prostate Specific Antigen Rapid Test Device/ Strip (Whole Blood/Serum/Plasma)
SUMMARYPSA has been detected in various tissues of the male urogenital system but only prostate glandular cells and endothelial cells secrete it. The PSA level in the serum of healthy men is between 0.1 ng/mL and 2.6 ng/mL. It can be elevated in malignant conditions such as prostate cancer, and in benign conditions such as benign prostatic hyperplasia and prostatitis. A PSA level of 4 to 10 ng/mL -
Dengue IgG/IgM Rapid Test Device with CE ISO13485
PrincipleThe Dengue IgG/IgM Rapid Test Device (Whole Blood/Serum/Plasma) is a qualitative membrane‐based immunoassay for the detection of Dengue antibodies in whole blood, serum, or plasma. This test consists of two components, an IgG component and an IgM component. In the Test region, anti‐human IgM and IgG is coated.During testing, the specimen reacts with Dengue antigen‐coated particles in the -
Ferritin Rapid Test Device (whole blood/serum/plasma)
PRINCIPLEThe Human Ferritin Rapid Test Device (Whole blood/Serum/Plasma) is a qualitative, lateral flowimmunoassay for the detection of human Ferritin in human whole blood, serum and plasma. Themembrane is pre‐coated with anti‐ferritin antibody on the test line region of the strip. Duringtesting, the specimen reacts with the particle coated with anti‐ferritin antibody. The mixturemigrates upward o -
Chlamydia Rapid Test Device
PrincipleIt is a qualitative, lateral flow immunoassay for the detection of Chlamydia antigen from clinical specimens. In this test, antibody specific to the Chlamydia antigen is coated on the test line region of the strip. During testing, the extracted antigen solution reacts with an antibody to Chlamydia that is coated onto particles. The mixture migrates up to react with the antibody to Chlamyd -
Monkeypox virus IgG/IgM Rapid Test
KIT COMPONENTS• Test devices• Droppers• Single Buffer• Package insertPrincipleThe Monkeypox virus IgG/IgM Rapid Test is a qualitative membrane-based immunoassay for the detection of Monkeypox antibodies in whole blood, serum, or plasma. This test consists of two components, an IgG component and an IgM component. In the IgG component, anti-human IgG is coated in test line region G of the test. Duri -
COVID-19 IgG/IgM Rapid Test Device
INTENDED USEThe COVID-19 IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG anti–COVID-19 virus and IgM anti-COVID-19 virus in human whole blood, serum or plasma. It is intended to be used by the professionals as a screening test and as an aid in the diagnosis of infection with COVID-19 viruses. Any reactive specimen with the COVID-19 IgG/IgM -
Monkeypox AG Rapid Test Cassette (Swab)
KIT COMPONENTS• Test devices• Droppers• Single Buffer• Package insertPrincipleMonkeypox is a rare disease that is caused by infection with monkeypox virus. The first human case of monkeypox was recorded in 1970 in the Democratic Republic of the Congo (DRC) during a period of intensified effort to eliminate smallpox. Since then, monkeypox has been reported in people in several other central and wes -
COVID-19 Ag Rapid Test Device
KIT COMPONENTS20 test cassette20 sterile swabs20 single extraction buffer1 package insert1 quick referance guidePRODUCT SPECIFICATIONBrandFunworldCertificateCE , ISO13485SpecimenNasopharyngeal swabs/ Nasal swabContentsCassette , Buffer , sterile swabs Package insertReading time10 minutesPack20 TStorage2-30℃Shelf life2 YearsORDERIING INFORMATION Product describtionSpecimenFormatPackCertificateSARS -
HIV Ab/Ag Human Immunodeficiency Virus Rapid Test Kit
PrincipleThe HIV 1/2 Human Immunodeficiency Virus Rapid Test Device (Whole Blood/Serum/Plasma) is a qualitative, membrane based immunoassay for the detection of antibodies to HIV 1/2 in whole blood, serum or plasma. The membrane is pre‐coated with recombinant HIV antigens. During testing, the whole blood, serum or plasma specimen reacts with HIV antigen coated particles in the test strip. The mixt -
SARS-CoV-2 Neutralizing Antibody Rapid Test Device
KIT COMPONENTSIndividually packed test devicesEach device contains a strip with colored conjugates and reactive reagents pre-spreaded at the corresponding regionsDisposable pipettesFor adding specimens useBufferPhosphate buffered saline and preservativePackage insertFor operation instructionASSAY PROCEDURERing the specimen and test components to room temperature Mix the specimen well prior to assa -
COC,OPI,MDMA,AMP,THC,BZO One Step Drug Test Test Device Saliva
INTENDED USEDuring testing, a urine specimen migrates upward by capillary action. Drug Test, if present in the urine specimen below 300 ng/mL, will not saturate the binding sites of the antibody coatedparticles in the test device. The antibody coated particles will then be captured by immobilizedDrug Test conjugate and a visible colored line will show up in the test line region. The colored line w -
OPI, MET, KET One Step Opiate Test Device
KIT COMPONENTS(Device)Individually packed Test DevicesEach device contains a strip with colored conjugatesand reactive reagents pre-spreaded at thecorresponding regions.Disposable pipettesFor adding specimens use.Package insertFor operation instruction.PROCEDUREBring tests, specimens and/or controls to room temperature (15-30°C) before use.1. Bring the pouch to room temperature before opening it.
