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Follicle Stimulating Hormone Fsh in Urine Sample Rapid Test
Overview Intended Use The FSH Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of Follicl;
Overview
The FSH Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of Follicle Stimulating Hormone (FSH) in urine to aid in the detection of menopause.
Menopause is the permanent cessation of menstruation but is usually not scientifically diagnosed until one full year after a woman's menstrual periods have stopped. The period leading up to menopause, and the 12 months following, is known as perimenopause. Many women experience symptoms during this time including hot flashes, irregular menstrual cycles, sleep disorders, vaginal dryness, hair loss, anxiety and mood swings, short-term memory loss and fatigue. The onset of perimenopause is caused by changes in the levels of hormones in the female body that regulate the menstrual cycle. As the body produces less and less estrogen, it increases its production of FSH, which normally regulates the development of a female's eggs. Therefore, testing for FSH can help determine whether a woman is in the perimenopause stage. If a woman knows she is perimenopausal, she can take the appropriate steps to keep her body healthy and avoid the health risks associated with menopause, which include osteoporosis, increased blood pressure and cholesterol, and increased risk of heart disease. The FSH Rapid Test Strip is a rapid test that qualitatively detects the FSH level in urine specimen at the sensitivity of 25 mIU/mL. The test utilizes a combination of antibodies including a monoclonal anti-FSH antibody to selectively detect elevated levels of FSH.
FSH Rapid Test with desiccant. Instruction manual
The urine specimen must be collected in a clean and dry container. A first morning urine specimen is preferred since it generally contains the highest concentration of FSH; however, urine specimens collected at any time of the day may be used. Urine specimens exhibiting visible precipitates should be centrifuged, filtered or allowed to settle to obtain a clear specimen for testing.
1. Remove test Strip, Device or Midstream from the sealed pouch. 2.1 Strip: Remove test strip from the sealed pouch. Dip the arrowed end of the test strip into the container with urine sample, take it out in 5 seconds and lay flat. 2.2 Device/Cassette: Remove test device/cassette from the sealed pouch. Lay the device flat, add 2-3 drops of urine specimen by sample dropper into the sample well. 2.3 Midstream/Pen: Remove test midstream from the sealed pouch. Open the midstream cup, dip the sample collection head into urine sample, take it out in 5 to 10 seconds and lay it flat. 3. Read the results within 5 minutes. Do not interpret the result after 10 minutes.
15% annual sales amount is devoted R&D department.With professional R&D team, Dewei is continuously making new achievements on innovation, gaining numbers of national invention patents and professional technical awards. Meanwhile, Dewei focuses on the improvement of technology to guarantee product quality and pursue product performance.
Transportation
Basic Info.
| Model NO. | FSH-DU02 |
| Usage | Professional Use |
| Certificate | ISO, CE |
| Transport Package | Cartons |
| Specification | 40test/box |
| Trademark | Dewei |
| Origin | China |
| Production Capacity | 100, 000PCS/Day |
Product Description
Intended Use
The FSH Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of Follicle Stimulating Hormone (FSH) in urine to aid in the detection of menopause.
Introduction
Menopause is the permanent cessation of menstruation but is usually not scientifically diagnosed until one full year after a woman's menstrual periods have stopped. The period leading up to menopause, and the 12 months following, is known as perimenopause. Many women experience symptoms during this time including hot flashes, irregular menstrual cycles, sleep disorders, vaginal dryness, hair loss, anxiety and mood swings, short-term memory loss and fatigue. The onset of perimenopause is caused by changes in the levels of hormones in the female body that regulate the menstrual cycle. As the body produces less and less estrogen, it increases its production of FSH, which normally regulates the development of a female's eggs. Therefore, testing for FSH can help determine whether a woman is in the perimenopause stage. If a woman knows she is perimenopausal, she can take the appropriate steps to keep her body healthy and avoid the health risks associated with menopause, which include osteoporosis, increased blood pressure and cholesterol, and increased risk of heart disease. The FSH Rapid Test Strip is a rapid test that qualitatively detects the FSH level in urine specimen at the sensitivity of 25 mIU/mL. The test utilizes a combination of antibodies including a monoclonal anti-FSH antibody to selectively detect elevated levels of FSH.
Contents
FSH Rapid Test with desiccant. Instruction manual
Storage & Statibility
- The kit should be stored at 2-30°C until the expiry date printed on the sealed pouch.
- The test must remain in the sealed pouch until use.
- Keep away from direct sunlight, moisture and heat.
- Do not freeze.
- Care should be taken to protect the components of the kit from contamination. Do not use if there is evidence of microbial contamination or precipitation. Biological contamination of dispensing equipment, containers or reagents can lead to false results.
Sample Collection&Storage
The urine specimen must be collected in a clean and dry container. A first morning urine specimen is preferred since it generally contains the highest concentration of FSH; however, urine specimens collected at any time of the day may be used. Urine specimens exhibiting visible precipitates should be centrifuged, filtered or allowed to settle to obtain a clear specimen for testing.
Operation
1. Remove test Strip, Device or Midstream from the sealed pouch. 2.1 Strip: Remove test strip from the sealed pouch. Dip the arrowed end of the test strip into the container with urine sample, take it out in 5 seconds and lay flat. 2.2 Device/Cassette: Remove test device/cassette from the sealed pouch. Lay the device flat, add 2-3 drops of urine specimen by sample dropper into the sample well. 2.3 Midstream/Pen: Remove test midstream from the sealed pouch. Open the midstream cup, dip the sample collection head into urine sample, take it out in 5 to 10 seconds and lay it flat. 3. Read the results within 5 minutes. Do not interpret the result after 10 minutes.
Detailed Photos
Company Profile
About Us
Dewei Medical Equipment Co., Ltd. is a high-tech enterprise specialized in developing and marketing of Medical Consmuables like Clinical Laboratory analyzer and reagents, Hematology Analyzer and Reagents, Washing Solutions, Urine Sediment Reagents and DNA/RNA Preservation Kits.During the special period of Corona, Dewei also develop the reagent kits, like Virus Transport Medium with swab, Rapid test and Saliva Collection Kits.Dewei products are widely used in hospital clinics, disease control centers, blood banks, veterinary clinics, scientific research center and college laboratories.
15% annual sales amount is devoted R&D department.With professional R&D team, Dewei is continuously making new achievements on innovation, gaining numbers of national invention patents and professional technical awards. Meanwhile, Dewei focuses on the improvement of technology to guarantee product quality and pursue product performance.
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