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Accuracy 99.9% Midstream FSH Rapid Test Follicle Stimulating Hormone Detection

China Accuracy 99.9% Midstream FSH Rapid Test Follicle Stimulating Hormone Detection

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Accuracy 99.9% Midstream FSH Rapid Test Follicle Stimulating Hormone Detection

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Supply Ability	10 M tests/month
Delivery Time	2-4 Weeks
Packaging Details	50T
Format	Dipstick
Product	FSH Rapid Test Midstream Rapid Test Kits Detection For Follicle Stimulating Hormone-Dipstick
Cat No.	FFS-101/111
Principle	Chromatographic Immunoassay
Certificate	CE/CE0123
Reading Time	3 minutes
Pack	50T
Sensitivity	＞99.9%
Specificity	＞99.9%
Accuracy	＞99.9%
Cut-Off	25 mIU/mL
Features 1	Fast results
Features 2	Easy visually interpretation
Features 3	Simple operation, no equipment required
Features 4	High accuracy
Brand Name	Citest
Model Number	FFS-101/111
Certification	CE/CE0123
Place of Origin	-

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Product Details
Company Details

Product Specification


Supply Ability	10 M tests/month	Delivery Time	2-4 Weeks
Packaging Details	50T	Format	Dipstick
Product	FSH Rapid Test Midstream Rapid Test Kits Detection For Follicle Stimulating Hormone-Dipstick	Cat No.	FFS-101/111
Principle	Chromatographic Immunoassay	Certificate	CE/CE0123
Reading Time	3 minutes	Pack	50T
Sensitivity	＞99.9%	Specificity	＞99.9%
Accuracy	＞99.9%	Cut-Off	25 mIU/mL
Features 1	Fast results	Features 2	Easy visually interpretation
Features 3	Simple operation, no equipment required	Features 4	High accuracy
Brand Name	Citest	Model Number	FFS-101/111
Certification	CE/CE0123	Place of Origin	-
High Light	Accuracy 99.9% Midstream FSH Rapid Test ，Accuracy 99.9% FSH Rapid Test ，99.9% Follicle Stimulating Hormone Detection Dipstick

FSH Rapid Test Midstream Rapid Test Kits Detection For Follicle Stimulating Hormone-Dipstick

Principle	Chromatographic Immunoassay
Format	Dipstick, Cassette, Midstream
Specimen	Urine
Certificate	CE/CE0123
Reading Time	3 minutes
Pack	2T/40T/50T
Storage Temperature	2-30°C
Shelf Life	2 Years
Sensitivity	＞99.9%
Specificity	＞99.9%
Accuracy	＞99.9%
Cut-Off	25 mIU/mL

The FSH Rapid Test Dipstick (Urine) is a rapid chromatographic immunoassay for the qualitative detection of follicle stimulating hormone (FSH) in urine to aid in the detection of menopause.

SUMMARY

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 estro/gen, 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 Dipstick 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.

PRINCIPLE

The FSH Rapid Test Dipstick is a qualitative, lateral flow immunoassay for the qualitative detection of human Follicle Stimulating Hormone in urine to evaluate the onset of menopause in women. The test utilizes a combination of antibodies including a monoclonal anti-FSH antibody to selectively detect elevated levels of FSH.

The assay is conducted by immersing the test strip in a urine specimen and observing the formation of colored lines. The specimen migrates via capillary action along the membrane to react with the colored conjugate. Positive specimens react with the specific antibody-FSH colored conjugate to form a colored line at the test line region of the membrane which is darker than or the same shade as the line in the control line

region.

To serve as a procedural control, a colored line will always appear in the control line region, indicating that the proper volume of specimen has been added and membrane wicking has occurred

DIRECTIONS FOR USE

Allow the test, urine specimen and/or controls to reach room temperature (15- 30°C) prior to testing.

1. Determine the day to begin testing. (See the above section: “WHEN TO START TESTING”).

2. Bring the pouch or closed canister to room temperature before opening it. Remove the test dipstick from the sealed pouch or closed canister and use it as soon as possible.

NOTE: For canister packaging, immediately close the canister tightly after removing the required number of the test dipstick(s). Record the initial opening date on the canister. Once the canister has been opened, the remaining test dipstick(s) are stable for 90 days only.

3. With arrows pointing toward the urine specimen, immerse the test dipstick vertically in the urine specimen for at least 10-15 seconds. Do not pass the maximum line (MAX) on the test dipstick when immersing the dipstick. See illustration below.

4. Place the test dipstick on a non-absorbent flat surface, start the timer and wait for the colored line(s) to appear. Read results at 3 minutes. Do not interpret the result after 10 minutes.

INTERPRETATION OF RESULTS

(Please refer to the illustration above)

POSITIVE: Two lines are visible and the line in test line region (T) is the same as or darker than the line in the control line region (C). A positive result means that the FSH level is higher than normal. Record the results and see the chart below to interpret results.

NEGATIVE: Two lines are visible, but the line in the test line region (T) is lighter than the line in the control line region (C), or there is no line in the test line region (T). A negative result means that the FSH level is not elevated at this time.

Record the results and see the chart below to interpret results.

INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

Sensitivity and Specificity

The FSH Rapid Test Dipstick can detect FSH at concentrations of 25 mIU/mL or greater. The addition of LH (1,000 mIU/mL), hCG (100 mIU/mL), and TSH (1,000 µIU/mL) to negative (0 mIU/mL FSH) and positive (25 mIU/mL FSH) specimens showed no cross-reactivity

Positive Agreement: 100.0% (96.6%-100.0%)*

Negative Agreement: 100% (95.7%-99.9%)*

Overall Agreement: 100% (97.1%-99.9%)*

*95% Confidence Interval

Order Information

Cat. No.	Product	Specimen	Pack
FFS-101	FSH Rapid Test Dipstick	Urine	50T
FFS-102	FSH Rapid Test Cassette	Urine	40T
FFS-103	FSH Rapid Test Midstream	Urine	2T
FFS-101H	FSH Rapid Test Dipstick(Self-Testing)	Urine	2T
FFS-102H	FSH Rapid Test Cassette(Self-Testing)	Urine	2T
FFS-103H	FSH Rapid Test Midstream(Self-Testing)	Urine	2T

Company Details

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Business Type:

Manufacturer,Exporter,Trading Company 
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Total Annual:

80000000-100000000
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Employee Number:

500~10000 
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Ecer Certification：

Verified Supplier 

CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies. ... CITEST DIAGNOSTICS INC., an emerging In Vitro Diagnostics company based in Canada, is experiencing growth on a global scale, engaging in multinational operations. CITEST was founded by highly experienced IVD industry professionals with proven track records building and growing successful companies. ...

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CITEST DIAGNOSTICS INC.
170-422, Richards Street, Vancouver BC V6B 2Z4, CANADA
https://www.citesttestkit.com/

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