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Dengue IgG/IgM Rapid Test Device with CE ISO13485
Dengue viruses, a family of four distinct serotypes of viruses (Den 1,2,3,4), are single‐strained, enveloped, positive‐sense RNA viruses.
The test is user friendly, without cumbersome laboratory equipment, and requires minimal staff trainings. -
Chlamydia Rapid Test Device
The Chlamydia Rapid Test Device is a rapid chromatographic immunoassay for the qualitative detection of Chlamydia trachomatis in clinical specimens to aid in the diagnosis of Chlamydia infection.
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Monkeypox virus IgG/IgM Rapid Test
The Monkeypox virus IgG/IgM Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to Monkeypox virus in human whole blood, serum, or plasma as an aid in the diagnosis of Monkeypox infections.
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Monkeypox AG Rapid Test Cassette (Swab)
Monkeypox Ag Rapid Test Cassette (Swab) is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of monkeypox virus antigen in human throat or vesicle /acne scab focus swab specimen. This test provides only a preliminary test result. Therefore, any reactive specimen with the Monkeypox Ag Rapid Test Cassette (Swab) must be confirmed with alternative testing method(s) and clinical findings.
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HIV Ab/Ag Human Immunodeficiency Virus Rapid Test Kit
Human Immunodeficiency Virus (HIV) Ab & P24 Ag Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of antibodies to HIV 1 and/or HIV 2 and P24 antigen in whole blood, serum or plasma.HIV is the etiologic agent of Acquired Immune Deficiency Syndrome (AIDS). The virion issurrounded by a lipid envelope that is derived from host cell membrane. Several viralglycoproteins are on the envelope. Each virus contains two copies of positive-sense genomicRNAs. HIV 1 has been isolated from patients with AIDS and AIDS-related complex, and fromhealthy people with high potential risk for developing AIDS.1 HIV 2 has been isolated from WestAfrican AIDS patients and from seropositive asymptomatic individuals.2 Both HIV 1 and HIV 2elicit immune response.3 Detection of HIV antibodies in serum, plasma or whole blood is themost efficient and common way to determine whether an individual has been exposed to HIVand to screen blood and blood products for HIV.4 Despite of the differences in their biologicalcharacters, serological activities and genome sequences, HIV 1 and HIV 2 show strong antigeniccross-reactivity.5,6 Most HIV 2 positive sera can be identified by using HIV 1 based serologicaltests. Dogma predicts, however, that a viral protein like p24 should be at least as good a markerof HIV disease activity, provided that it is measured with sufficient sensitivity and accuracy.Human Immunodeficiency Virus (HIV) Ab & P24 Ag Rapid Test Device (WholeBlood/Serum/Plasma) is a rapid test to qualitatively detect the presence of antibody to HIV 1and/or HIV 2 and P24 antigen in whole blood, serum or plasma specimen. The test utilizes latexconjugate and multiple recombinant HIV proteins to selectively detect antibodies to the HIV 1&2and P24 antigen in whole blood, serum or plasma. -
COC,OPI,MDMA,AMP,THC,BZO One Step Drug Test Test Device Saliva
The Drug Test Test Device Saliva is a lateral flow chromatographic immunoassay for the detection of Drug Test in human Saliva. This test will detect other compounds, please refer to Analytical Specificity table in this package insert.
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OPI, MET, KET One Step Opiate Test Device
The OPI One Step Opiate Test Device (Urine) is a lateral flow chromatographic immunoassay for the detection of Drug Test in human urine at the cut-off concentration of 2,000 ng/mL. This test will detect other related compounds, please refer to the Analytical Specificity table in this package insert. This assay provides only a qualitative, preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.
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SARS-CoV-2 Antigen Rapid Test Device (Saliva)
INTENDED USE The SARS-CoV-2 Antigen Rapid Test device is a rapid visual immunoassay for the qualitative, presumptive detection of SARS-CoV-2 antigens form Nasal swabs specimens. The test is intended for use as an aid in the rapid differential diagnosis of acute SARS-CoV-2 virus infection. PRINCIPLE The detection of SARS-COV-2 adopts the principle of double antibody sandwich method and colloidal gold immunochromatography to qualitatively detect SARS-COV-2 antigen in human Nasopharyng... -
SARS-CoV-2 Antigen Rapid Test Device(Self-Testing)
The SARS-CoV-2 Antigen Rapid Test device is a rapid visual immunoassay for the qualitative, presumptive detection of SARS-CoV-2 antigens form Nasal swabs specimens. A nasal swab sample can be self-collected by an individual aged 15-70 years. People between the ages of 15 and 70 who are unable to collect samples by themselves may be assisted by other adults. The test is intended for self-testing use as an aid in the rapid differential diagnosis of acute SARS-CoV-2 virus infection.
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Multi drug Test Panel with CE ISO
1 Brand: Funworld
1 Specimens: : Urine
Reading time：5 minutes.
Pack：CustomizedSTORAGE: 2‐30°C
Certification: CE, ISO 13485
KIT COMPONENTS(Device)
· Test device
· Disposable pipettes
· Package insertThe Rapid Response Drugs of Abuse Test Device is a rapid visual immunoassay for the qualitative, presumptive detection of drugs of abuse in human urine specimens at the cut-off concentrations listed below:
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fFN Rapid Test Strip Manufacturer with Best Price
Brand: Funworld
Specimens: Vaginal secretion
Reading time：10 minutes.
Pack：20T
STORAGE: 2‐30°C
KIT COMPONENTS(Device)
Individually packed test strips
Specimens collection swab
Specimens dilution tube with buffer
Package insert
The fetal fibronectin (fFN) rapid test (vaginal secretion) is a visually interpreted, qualitative immunochromatographic test device for detection of fFN in vaginal secretions during pregnancy, which is a special protein that literally holds your baby in place in the womb. The test is intended for professional use to help diagnose the rupture of fetal membranes (ROM) in pregnant women. -
Funworld fFN Rapid Test Device for Wholesale
The fetal fibronectin (fFN) rapid test (vaginal secretion) is a visually interpreted, qualitative
immunochromatographic test device for detection of fFN in vaginal secretions during pregnancy, which is a special protein that literally holds your baby in place in the womb. The test is intended for professional use to help diagnose the rupture of fetal membranes (ROM) in pregnant women.
