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  • Product Name: Ovulation Test strip
  • null(en)
    型号规格 LH-A3.5 50条装
【Common name】 Luteinizing hormone test paper (colloidal gold immunochromatography)
【English name】 Luteinizing Hormone (LH) Test Strip (Colloidal gold immune chromatography)
【Product name】 Ovulation test strip 50 tests/ box
【Main Composition】
From the test strip and its support composition, test strips on the main components are:
A) Anti-luteinizing hormone (LH) antibody (immobilized on a nitrocellulose membrane);
B) Anti-mouse IgG polyclonal antibody (immobilized on nitrocellulose membrane);
C) Colloidal gold-labeled anti-LH monoclonal antibodies (immobilized on glass fibers);
D) Other test strip supports.
Other test paper accessories, such as straws, desiccants and so on.
【Storage conditions and validity】
Stored at 2 to 30 degrees Celsius from dark, self-test qualified from the date of validity of 36 months, Kaifeng should be used immediately.
【Sample Requirement】
From the beginning of the test date, try to use the same time every day urine test, in order to compare the test results (preferably in the morning after getting up, with the first urine test), 2 hours before the test should avoid drinking water And other water intake, because the water will dilute the concentration of LH in vivo, hinder the determination of LH peak.
【Testing method】
1. Collect urine from a clean, dry container (eg, such as an attached urine cup).
2. Prepare the chronograph, use only when the aluminum foil bag along the notch tear, remove the test strip.
3. The test strip labeled "MAX" end into the urine, the urine interface does not exceed the test strip arrow marks the line.
4. three seconds after the test strip, flat, wait until 8 minutes to observe the results of the middle of the test strip. (Too long or too short may affect the determination of test results)
【Manufacturer】
BCT Systems Co., Ltd.
Registration, production Address: 4F & Right side of 2F, No.3 Lady Road,Fucheng, Longhua , Shenzhen.
Postal Code: 518110
【Medical Device Manufacturer License No.】
Guangdong Drug Administration Department Production Permit  No. 20041005
【Medical device registration certificate No.】
Guangdong Device Registration No. 20162401059
【Technical requirements for medical instruments】
Guangdong Device Registration No. 20162401059


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