Brief:Qualitative detection the content of Total Prostate Specific Antigen (tPSA) in human blood specimen. An auxiliary diagnostic method for screening and detecting prostate cancer for men.
Brief: Rapid Initial and Qualitative Diagnostic Testing of Chlamydia Trachomatis Antigen. For Male and Female Suspected Infected Person Use. Specimen: Cervical swab/Urethral swab. Valid for 24 months. FOR PROFESSIONAL CLINICAL USE.
Brief: Rapid Qualitative Diagnostic Testing of HIV 1&2 Antibody. For Male and Female Suspected Infected Person Use. Specimen: Serum/Plasma/Whole blood. Valid for 24 months. FOR PROFESSIONAL CLINICAL USE.
Brief:HE4 Rapid Test Kit is used to detect Human Epididymis Erotein 4 (HE4) in human blood samples and is used clinically to monitor the efficacy of ovarian cancer.
Brief: Effective and High Accuracy 8-in-1 Respiratory Viral Panel Test Kit. Detect SARS-CoV-2/Flu A+B/HPIV/RSV/ADV/MP/Strep A from human Oropharyngeal Swab Specimens. 1 Test, 8 Results. CE Certified. Valid for 24 months.(The production date is customizable.) Stored at room temperature at 2~30℃.
Brief:CA15-3 Rapid Test Kit is used to detect Cancer Antigen CA15-3 in human samples, and mainly used in Clinical Observation of Therapeutic Efficary and Prognosis of Breast Cancer.
Brief:High Accuracy, Efficient and Rapid Antigen Test Kit. Easy at Home for Self Diagnostic Testing. Detect 7 types Respiratory Multiple Pathogens in 15 Minutes.
Brief:This product is used for in vitro qualitative detection of Sars-Cov-2(Covid-19) antigens. This product has been approved by FDA/EUA. This product is only available in the US market. Sales method: Wholesale Only Min Order: 2 cartons (about 1200 boxes)
Brief:This kit is only used for the invitro qualitative detection of Influenza A virus and Influenza B virus from human anterior nasal swab specimens.Flu A/Flu B Antigen Rapid Test Kit (immunochromatographicassay) is an immunochromatographic double-antibody sandwich assay intended for the qualitative detection and differentiation of Influenza A virus and Influenza B virus from individuals who are suspected of respiratory tract disease infection. This kit is suitable for the auxilary diagnosis of respiratory diseases,the results are for clinical reference only and cannot be used as the sole basis for diagnosis and exclusion decision.The clinical diagnosis and treatment of patients should be considered in combination with their symptoms/signs,medical history,other laboratory tests and treatment responses.Positive test result needs to be further confimed,negative result does not preclude respiratory diseases viruses infection.
Brief: This kit is only used for the in vitro qualitative detection of Mycoplasma pneumoniae from human oropharyngeal swab specimens. MP Antigen Rapid Test Kit is an immunochromatographic double-antibody sandwich assay intended for the qualitative detection and differentiation of Mycoplasma pneumoniae from individuals who are suspected of respiratory tract disease infection.
Brief: Qualitative detection of HPV virus from urine specimens. Total coincidence rate: 98%. CE certified. 1 test/kit; 600 tests/carton. Valid for 24 months. Only for in vitro diagnosis.
Brief:This kit is used for in vitro qualitative detection of high-risk and low-risk human papillomavirus (HPV) in vaginal swabs and cervical exfoliated cells. The high-risk HPV includes type 16,18,26,31,33,35,39,45,51,52,53,56,58,59,66,68,73,82; the low-risk HPV includes type 6,11,40,42,43, 44,54,61.
Brief: Using Chromatographic Immunoassay for Qualitative Detection of Early Pregnancy. Using Saliva to aid diagnosis of Early Pregnancy. Accuracy 99.76%. CE Certified. Patented Product.
Brief:This product uses double antibody sandwich immunochromatography technology to achieve in vitro qualitative detection of HCG in Human urine,which is not used for the detection of trophoblastic tumors.
Brief:The Candida albicans antigen rapid test kit is suitable for the in vitro qualitative detection of Candida albicans antigen in swabs of vaginal secretions from women over 18 years of age for the auxiliary diagnosis of Candida albicans infection.
Brief: Quick and Accurate qualitative diagnostic testing of Trichomonas Vaginalis antigen. Spicemen: Vaginal swab. Valid for 24 months. CE approved. For PROFESSIONAL USE.
