A rapid test for measuring Menopause in whole blood /serum /plasma with the use of Fiatest ^TMGofluorescence Immunoassay Analyzer. For professional in vitro diagnostic use only.

Application:

CRP Test Cassette (WB/S/P) is based on Fluorescence Immunoassay for the quantitative determination of C-reactive protein (CRP) in serum, plasma or whole blood as an aid in the evaluation of infection, tissue injury and inflammatory disorders along with measurement of high sensitivity CRP (hs-CRP) for evaluation of acute coronary syndromes (ACS).

Description:

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.1-3. 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.4,5

The FSH Test cassette is a rapid test that quantitatively detects the FSH level in Whole Blood /Serum/Plasma specimen. The test utilizes a combination of antibodies including a monoclonal anti-FSH antibody to selectively detect elevated levels of FSH. The minimum detection level is 10mIU/mL.

How to use?

Refer to Fiatest ^TMGo Fluorescence Immunoassay Analyzer Operation Manual for the complete instructions on use of the Test. The test should be in room temperature.

1. Turn on the Analyzer power. Then according to the need, select “Standard test” or “Quick test” mode.

2. Take out the ID card and insert it into the Analyzer port.

3. Serum or plasma: Pipette 5 μLserum or plasma into the buffer tube, mix the specimenand the buffer well.

Whole blood: Transfer 7.5 μLwhole blood into the buffer tube with sampler provided or pipette; mix the specimen and the buffer well.

4. Add diluted specimen with a Pipette: Pipette 75 μL diluted specimen into the sample well of the cassette. Start the timer at the same time.

Add specimen with sampler provided: Discard the first 2 drops, then add 2 drops of dilutedspecimen into the sample well of the cassette. Start the timer at the same time.

5. There are two test modes for Fiatest ^TMGo Fluorescence Immunoassay Analyzer, Standard Test mode and Quick Test mode. Please refer to the user manual of Fiatest ^TMGo Fluorescence Immunoassay Analyzer for details.

“Quick test” mode: Insert the test cassette into the Analyzer at 3 minutes after sample application click “QUICK TEST”, fill the test information and click "NEW TEST" immediately. the Analyzer will automatically give the test result after a few seconds.

“Standard test” mode: Insert the test cassette into the Analyzer immediately after sample application, click “STANDARD TEST”, fill the test information and click "NEW TEST" at the same time, the Analyzer will automatically counting down 3 minutes. After the countdown, the Analyzer will give the result at once.

INTERPRETATION OF RESULTS
Results read by Fiatest ^TMGo Fluorescence Immunoassay Analyzer.
The result of tests for C-reactive Protein is calculated by Fiatest ^TMGoFluorescence Immunoassay
Analyzer and display the result on the screen. For additional information, please refer to the user
manual of Fiatest ^TMGo Fluorescence Immunoassay Analyze.
Linearity range of FluroLit TM CRP is 0.5-200 mg/L.

Catalogue Number	Item Name	Sample	Test Range	KIT size
FI-CRP-402	CRP Test Cassette	WB/S/P	0.5~200 mg/L	10T/25T

Tag:

Place of Origin:	China
Brand Name:	Fiatest Go
Certification:	CE, ISO13485
Model Number:	FI-FSH-402

Minimum Order Quantity:	N/A
Price:	Negotiation
Packaging Details:	10T/25T
Delivery Time:	2-4 Weeks
Payment Terms:	Ex works
Supply Ability:	10 M tests/month

Format:	Cassette	Specimen:	Whole Blood /serum /plasma
Kit Size:	10T/25T	Storage:	2-30℃
Test Range:	0.5~200 Mg/L	Certificate:	CE
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	Hangzhou AllTest Biotech CO.,LTD
	#383, Qiaoxin Road, Xiasha Street, Qiantang Disctrict, Hangzhou, Zhejiang, P.R.China
	86-571-56267891
	selina.wu@alltests.com.cn

Menopause Test Use By Fiatest GO Fluorescence Immunoassay Analyzer In Human Whole Blood

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