Product Details:
Number of Reactions(Preps)/Kit : 25 T
Brand : Boditech Med Incorporated
Sample : whole blood (AFIAS), plasma, serum
Reaction Time : 15mins
Detection Range : ichroma(TM) (1 - 100 mIU/ml)
Cat No : CEPC-35
Follicle-stimulating Hormone (FSH)
Diagnosis of early menopause & ovarian degeneration and infertility
This test can help figure out the cause of infertility, problems with ovarian functions, menstrual abnormalities and congenital or acquired gonadotropin development disorder or infertility.
Home Menopause Test Strip is an in vitro diagnostic (IVD) qualitative test for rapid detection of human Follicle Stimulating Hormone (FSH) in urine at a sensitivity of 25mIU/ml. SUMMARY AND EXPLANATION OF THE TEST Follicle Stimulating Hormone (FSH) is a peptide hormone produced in the pituitary gland of the brain. It is normally present in the blood or urine varying in concentration with the stage of the menstrual cycle. When estrogen levels drop, FSH is released from the pituitary gland indicating that either a woman in mid-menstrual cycle or the onset of perimenopause. During early menopause, changes take place in the balance of hormones that regulate and control menstrual cycles. As a woman grows older and passes out of childbearing stage of life, the ovaries gradually make less of the hormone estrogen and FSH increases.FSH normally regulates the growth and development of an egg. Once this part of the monthly cycle is complete, FSH production is stopped and it returns to normal. As the body decreases estrogen production with age, more FSH is made. Over time these hormone changes cause menstrual periods to stop completely and "menopause" has occurred. The slow change in ovary function can happen between 2 and 10 years before the final period. This early stage before menopause is called perimenopause. During this stage, the levels of FSH may rise to positive levels and slowly return to normal, causing irregular or missed periods. The testing for FSH should be performed twice to help identify the levels of FSH throughout a menstrual cycle. PRECAUTION 1. For in vitro diagnostic use only. 2. Do not use after expiration date. 3. Test device should remain sealed until ready for use. Do not use if pouch is damaged or opened. 4. Read this instruction carefully before performing the test. 5. Do not re-use the test device. 6. Do not eat the desiccant in the pouch.
CE Approved The Follicle Stimulating Hormone (FSH) Test Kit is a rapid qualitative test for detect FSH in urine. This help to check the function of the pituitary gland and check if hormone levels are normal. The test can be used to see if a woman has started the menopause. The test may also be used (along with other tests) for detecting possible causes of both male and female infertility. Self-detection of ovarian function Guide to prevention of premature ovarian Diagnosis of menopause
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : Human serum/plasma/ control Specimen volume : 75 Microliter stored at ; 4 - 30 DegreeC Cat No ; CFPC-44 T3 Assessing to diagnosis & to monitor thyroid diseases(T3) This test assesses the level of T3 in the blood to diagnose thyroid dysfunction, help to receive appropriate treatment, and help to confirm the treatment effect through periodic measurement. INTENDED USE : ichroma T3 is a fluorescence Immunoassay (FIA) for the quantitative determination of triiodothyronine (total T3) in human serum/plasma. It is useful as an aid in management and monitoring of determination of thyroid disorders. For in vitro diagnostic use only. PRINCIPLE : The test uses a competitive immunodetection method. In this method, the analyte in the sample binds to the fluorescence labeled (FL) detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of T3 and bovine serum albumin (BSA) is immobilized and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated, resulting in less fluorescence signal. MATERIALS SUPPLIED : REF CFPC-44 Components of ichroma T3 Cartridge Box: - Cartridge 25 - Detector tube 25 - Detector diluent 2 - ID chip 1 - Instruction for Use 1
Product Details: Brand : Boditech Med Incorporated Size : 25 T Specimen : Human serum/plasma/ control Specimen volume : 75 microliter stored at 4 - 30 DegreeC. Cat No : CFPC-26 T4 Assessing to diagnosis & to monitor thyroid diseases(T4) Thyroxine (T4) is a type of thyroid hormone. An abnormal amount of T4 may indicate thyroid disease. The T4 test measures total T4, including T4 bonded to protein and free T4. A T4 test will help determine what type of problem is affecting the thyroid. INTENDED USE : ichroma T4 is a fluorescence Immunoassay (FIA) for the quantitative determination of thyroxine (T4) in human serum/plasma. It is useful as an aid in management and monitoring of thyroid disorder. For in vitro diagnostic use only. PRINCIPLE : The test uses a competitive immunodetection method. In this method, the target material in the sample binds to the fluorescence (FL)-labeled detection antibody in detector, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of T4 and bovine serum albumin (BSA) is immobilized on a test strip, and interferes with the binding of target material and FL-labeled antibody. If the more target material exists in blood, the less detection antibody is accumulated, resulting in the less fluorescence signal. MATERIALS SUPPLIED : REF CFPC-26 Components of ichroma T4 Cartridge Box: - Cartridges 25 - ID Chip 1 - Insert 1 - Detector tube (Granule) 25 - Detector diluent (5.5 mL) 1
Product Details: Brand ; Boditech Med Incorporated Size : 25 T Samples: human whole blood/serum /plasma Specimen volume human whole blood/serum/ plasma stored at 4-30 C Cat. No. : CFPC-66 Human Chorionic Gonadotropin (�²-hCG) Distinguish pregnancy and abnormal pregnancy The IhCG test can be used to confirm pregnancy, the age of the fetus, abnormal pregnancy (ectopic pregnancy), potential miscarriage, and down syndrome. INTENDED USE : ichroma -HCG Plus is a fluorescence Immunoassay (FIA) for the quantitative determination of -HCG in human whole blood/serum /plasma. It is useful as an aid in management and monitoring of beta human chorionic gonadotropin (hCG) level in human For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; Dried antibodies in the detector tube, once diluted with the diluent, bind with antigens in the sample to form antigen-antibody complexes. These complexes then migrate through the nitrocellulose matrix and are captured by another sets of immobilized antibodies on the test line. The more antigens in the sample, the more antigen-antibody complexes, which leads to a stronger fluorescence signal. This signal then is interpreted by the reader to display the �²-HCG concentration in the sample. STORAGE AND STABILITY : The cartridge is stable for 20 months (while sealed in the original aluminum foil pouch) if stored at 4-30 C. The detector, diluent and sample diluent are stable for 20 months if stored at 2-8 C. After the cartridge pouch is opened, the test should be performed immediately. MATERIALS SUPPLIED : REF CFPC-66 Components of ichroma-HCG Plus Cartridge Box: - Cartridges 25 - ID Chip 1 - Instruction For Use 1 Buffer Box For ichorma II - Detectors (Capped with plastic lid) 25 - Diluent 1 For AFIAS-50 - Detectors (Sealed with aluminum foil) 25 - Diluent 1 Sample Diluent Box: - Sample Diluent Tubes 25
Product Details: Brand: Boditech Med Incorporated Size : 25 T Samples : human serum/plasma Specimen volume : 150 Microliter stored at 4 - 30 DegreeC. Cat. No : CFPC-22 Thyroid Stimulating Hormone (TSH) Diagnosing thyroid dysfunction One needs an adequate level of thyroid hormone. The excessive or insufficient level would cause various abnormalities in human physiology. The TSH test can deliver the required answer about the hormone level in 12 minutes with fingertip blood (US FDA 510k; AFIAS TSH). INTENDED USE : ichroma NT-proBNP is a fluorescence Immunoassay (FIA) for the quantitative determination of NT-proBNP in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of persons suspected of having congestive heart failure. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto the nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show NT-proBNP concentration in the sample. MATERIALS SUPPLIED : REF CFPC-77 Components of ichroma NT-proBNP Cartridge Box: - Cartridge 25 - ID Chip 1 - Instruction for Use 1 Buffer Box For ichroma II - Detector tube 25 - Detector diluent 1 For ichroma-50 - Detector tube 25 - Detector diluent 1
Product Details: Brand : Boditech Med Incorporated Size : 25 Test Samples : Whole blood Sample volume : 75 Microliter Cat No : CFPC-38 Storage Temperature ; 4 - 30 DegreeC HbA1c Assessing the level of glycated hemoglobin in the blood This test is certified by NGSP (National Glycohemoglobin Standardization Program). It helps diabetic diagnosis, treatment, and prognosis by measuring the glycated hemoglobin concentration (%) in a small amount of blood over the past 3 months. INTENDED USE ichroma HbA1c is a fluorescence Immunoassay (FIA) for the quantitative determination of HbA1c(Hemoglobin A1c) in human whole blood. It is useful as an aid in management and monitoring of the longterm glycemic status in patients with diabetes mellitus. For in vitro diagnostic use only. PRINCIPLE: The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody. Instrument for ichromaâ?¢ tests displays the content of glycated hemoglobin in terms of percent of the total hemoglobin in blood.
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : whole blood/serum/plasma Sample volume : 75 Microliter stored at 4 - 30 DegreeC Cat No i CHROMA PSA-25 Prostate Specific Antigen (PSA) Screening for the prostate cancer & monitoring the effects of the treatment This test helps in the early detection of prostate diseases such as enlarged prostate and prostatitis and prostate cancer by quantifying PSA in male blood, as well as observation of treatment effects and monitoring of recurrence.
Product Details: Brand ; Boditech Med Incorporated Size : 25 Test Samples : Serum/Plasma Recommended anticoagulant K2 EDTA, K3 EDTA, sodium heparin Storage Temperature : 4 - 30 DegreeC Cat No : CFPC-21 Progesterone Monitoring ovulation abnormalities and predicting miscarriage & ectopic pregnancy The progesterone test kit measures the level of progesterone in the blood. The progesterone test alone is not enough to diagnose a particular problem. But the result may help provide answers to causes of infertility, risk of miscarriage, ovulation, and ectopic pregnancy. PRINCIPLE : The test uses a competitive immunodetection method. In this method, the analyte in the sample binds to the fluorescence labeled (FL) detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of progesterone and bovine serum albumin (BSA) is immobilized, and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated, resulting in less fluorescence signal.