Home-Check Instant Ovulation Test is designed to detect the surge in Luteinizing Hormone (LH). The body always makes small amounts of LH but prior to ovulation it makes far more. This test device will detect the LH surge which happens in the middle of your menstrual cycle, about 1 -1.5 days before ovulation.
A pregnancy begins with conception. A child is conceived when the male sperm successfully fertilises the female egg. Successful fertilisation is most likely during a 24-hour period following the LH surge. Since this window is only open once a month and for a short period of time, being able to predict the L.H surge is very helpful when trying to become pregnant.
Home-Check Instant Ovulation test is highly accurate and sensitive. It can detect surge in LH levels as low as 20mlU/ml.
Hello, we are a manufacturer in China. There are 40,000 square meters of factory Welcome friends to visit If you want to buy, please contact us thanks Single use self-diagnostic ovulation test. This test is used to qualitatively detect LH (luteinizing hormone) in urine in order to predict the time of ovulation. Model:strip Efficiency: 99.98% Inner strip width: 3 mm Sensitivity: 25ml/miu Liquid moving speed: 10mm/ml Certificate: CE, ISO13485 Support small batch export Support mass customization Support exporting large boards Contact us for detailed pricing Looking forward to your contact
Our LH rapid test is based on the theory of enzyme interaction. It could be used to detect the content of LH atom in urine speciment. And the colour change will identify the result directly. Assisting with the result,doctor could judge whether the patient is pregnant . 2.5mm, 200 strips/pouch, 10,000strip /case ,27kg 3.0mm, 50 kits/ pouch, 2,000 kits/case, 27kg 4.0mm, 150 cards/pouch, 2,500 cards/case, 25kg 5.0mm 10000strips/case 2000kits/case 2500cards/case.
Supplier: Ovulation kit, menopause kit, pregnancy kit
Supplier: Diagnostic test kit, ovulation test kit test kit
Services: OEM
Supplier: Ovulation and pregnancy tests kits
Hello, we are a manufacturer in China. There are 40,000 square meters of factory Welcome friends to visit If you want to buy, please contact us thanks A single-use self-diagnostic pregnancy test. This test is used to qualitatively detect HCG (human chorionic gonadotropin) in urine for early detection of pregnancy. Model: strip, cassette, midstream Effective rate: 99.98%. Inner strip width: 3mmï¼?4mmï¼?6mm. Sensitivity: 25ml/miu Liquid moving speed: 10mm/ml Certificate: CE, ISO13485 Support small batch export Support mass customization Support exporting large boards Contact us for detailed pricing Looking forward to your contact
Products - Human Chorionic Gonadotropin (HCG) Test Midstream (Colloidal Gold Immunochromatographic Assay) Product Description - Sensitivity: 25 mIU/ml Accuracy: > 99.5% ISO13485 & CE approved INTENDED USE Easy-Sweet hCG Test Midstream is an in vitro diagnostic (IVD) qualitative test for rapid detection of hCG in urine. This test is designed for self-testing use only. PRINCIPLE Easy-Sweet. hCG Midstream is two-side sandwich immunoassay for the qualitative determination of human chorionic gonadotropin (hCG) in urine. The membrane was precoated with anti alpha hCG capture antibodies on the test band region and goat anti mouse on the control band region. During the test, the urine specimen is allowed to react with anti beta hCG monoclonal antibody-colloid gold conjugate, which was predried on the test Midstream. The mixture then moves forward on the membrane by the capillary action. For a positive specimen, the conjugate binds to the hCG forming an antibody-antigen complex. This complex is captured by anti alpha hCG antibody on the test region to produces a visual pink color band when hCG concentration in specimen is equal to or greater than 25 mIU/ml. Regardless of the presence of hCG, as the mixture continues to move across the membrane to the control band region, the complex is captured by immobilized goat anti mouse antibodies to form a distinct pink colored control band. The presence of the control band indicated: 1) a normal flow is obtained, 2) antibody pre-coated on control line and colloidal gold conjugate are functional. 1 pc/individual pouch , 500pcs/ctn or customized
What is Home-Check Menopause test? This is a home-use test kit to measure Follicle Stimulating Hormone (FSH) in your urine. This may help indicate if you are in menopause or perimenopause. Why should you do this Home-Check Menopause test? You should use this test if you want to know if your symptoms, such as irregular periods, hot flushes, vaginal dryness, or sleep problems are due to high levels of FSH which may be part of menopause. While many women may have little or no trouble when going through the stages of menopause, others may have moderate to severe discomfort and may want treatment to alleviate their symptoms. This test may help you be better informed about your current condition when you see your doctor. Key Features * Over 99% accurate* * Fast results – within minutes * Convenient * AUST L 174939 - approved by the TGA, European authorities and Indian FDA * Detects FSH levels higher than 25mlU/ml. Pack Contains: 1 In-stream Home-Check Menopause Menopause Test 1 Instruction Leaflet. Precautions: For external use only Always read the label Use only as directed. *In laboratory and consumer clinical studies.
Angiten-COVID-19 Virus Test Kit (Colloidal Gold) Quantity of box: 25 persons/box Brand: Easysweet NMPA (National Medical Products Administration): Approved CE: with CE mark BfArM: listed Test Method: Antigen Test Result Time: 10-15 mins Sample Type: Nasal Swab Sensitivity: 96.70% Specificity: 100% Accuracy: 98.94% Shelf Life: 24 months Storage Temperature: 2-30 Degree Celsius Country of Origin: Made in China Additional Information: Production Capacity: 1 million Delivery Time: 10-15 days Packaging Details: 25 tests in a pack, 40packs/ carton Angiten-COVID-19 Virus Test Kit is an in vitro diagnostic rapid test for the qualitative detection of SARS-CoV-2 antigen (Ag) in human nasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. It can be used by professional only.
