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>25MIU/mL Digital HCG Pregnancy Test Urine Detection Of HCG Human Chorionic

China 25MIU/mL Digital HCG Pregnancy Test Urine Detection Of HCG Human Chorionic

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25MIU/mL Digital HCG Pregnancy Test Urine Detection Of HCG Human Chorionic

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Product	Digital hCG Pregnancy Test, Detection of Human Chorionic Gonadotropin,Urine specimen
Principle	Chromatographic Immunoassay
Format	Midstream
Specimen	Urine
Certificate	CE0123
Reading Time	3 minutes
Pack	1T
Storage Temperature	2-30°C
Shelf Life	2 Years
Sensitivity	＞99.9%
Specificity	＞99.9%
Accuracy	＞99.9%
Cut-Off	25 mIU/mL
Brand Name	Citest
Model Number	FHC-E103H
Certification	CE0123
Place of Origin	-

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Product Specification


Product	Digital hCG Pregnancy Test, Detection of Human Chorionic Gonadotropin,Urine specimen	Principle	Chromatographic Immunoassay
Format	Midstream	Specimen	Urine
Certificate	CE0123	Reading Time	3 minutes
Pack	1T	Storage Temperature	2-30°C
Shelf Life	2 Years	Sensitivity	＞99.9%
Specificity	＞99.9%	Accuracy	＞99.9%
Cut-Off	25 mIU/mL	Brand Name	Citest
Model Number	FHC-E103H	Certification	CE0123
Place of Origin	-
High Light	25MIU/ML Digital HCG Pregnancy Test ，Urine Detection Of HCG ，hcg human chorionic gonadotropin test

Digital hCG Pregnancy Test, Detection of Human Chorionic Gonadotropin,Urine specimen

Principle	Chromatographic Immunoassay
Format	Midstream
Specimen	Urine
Certificate	CE0123
Reading Time	3 minutes
Pack	1T
Storage Temperature	2-30°C
Shelf Life	2 Years
Sensitivity	＞99.9%
Specificity	＞99.9%
Accuracy	＞99.9%
Cut-Off	25 mIU/mL

Application

Digital hCG Pregnancy Test is a rapid test for the qualitative detection of human chorionic gonadotropin (hCG) in in specimen to aid in the early detection of pregnancy.

Features

Self-testing format for High Privacy

Easy to use with 1 Step Operation

Over 99.9% Accuracy

Fast Results in 3 Minutes

Simple visually interpretation

PRECAUTIONS

Do not use after the expiration date printed on the foil pouch.
Store in a dry place at 2-30°C or 35.6-86°F. Do not freeze.
Do not use if pouch is torn or damaged
Keep out of the reach of children.
For in vitro diagnostic use. Not to be taken internally.
Do not open the test midstream foil pouch until you are ready to start the test.
The used test midstream should be discarded according to local regulations.

How to use?

1. Remove the midstream from the foil pouch and test them immediately in one hour.

2. Take down the cap of the midstream, hold the midstream so as to place the absorbent tip in the urine stream or place the absorbent tip (≥2/3) in urine in a clean cup for at least 15 seconds.

3. Cover the cap on the testing midstream, then lay down the products on a clean and stable desk, start the timer immediately.

4. Read the result at 3 minutes; don’t interpret the result after 10 minutes.

POSITIVE

Two distinct colored lines appear. One line should be in the control line region (C) and another line should be in the test line region (T). One line may be lighter than the other; they do not have to match. This means that you are probably pregnant.

NEGATIVE

One colored line appears in the control line region (C). No line appears in the test line region (T). This means that you are probably not pregnant.

INVALID

The result is invalid if no colored line appears in the control line region (C), even if a line appears in the test line region (T). You should repeat the

test with a new test midstream.

1. How does the test midstream work?

HCG Pregnancy Rapid Test Midstream detects a hormone in your urine that your body produces during pregnancy (hCG-human chorionic gonadotropin). The amount of pregnancy hormone increases as pregnancy progresses.

2. How soon after I suspect that I am pregnant can I take the test?

You can test your urine as early as the first day you miss your period. You can perform the test anytime of the day; however, if you are pregnant, first morning urine contains the most pregnancy hormone.

3. Do I have to test with first morning urine?

Although you can test at any time of the day, your first morning urine is usually the most concentrated of the day and would have the most hCG in it.

4. How accurate is the test?

A clinical evaluation was conducted comparing the results obtained using the HCG Pregnancy Rapid Test Midstream to another commercially available urine hCG test. The consumer clinical trial included 608 urine specimens: both assays identified 231 positive and 377 negative results. The results demonstrated >99% overall accuracy of the HCG Pregnancy Rapid Test Midstream when compared to the other urine hCG test.

5. How sensitive is the test?

HCG Pregnancy Rapid Test Midstream detects hCG in urine at a concentration of 25 mIU/mL or greater. The test has been standardized to the W.H.O. International Standard. The addition of LH (300 mIU/mL), FSH (1,000 mIU/mL), and TSH (1,000 µIU/mL) to negative (0 mIU/mL hCG) and positive (25 mIU/mL hCG) specimens showed no cross-reactivity.

6. What should I do if the result shows that I am pregnant?

It means that your urine contains hCG and you are probably pregnant. See your doctor to confirm that you are pregnant and to discuss the steps you should take.

7. How do I know that the test was run properly?

The appearance of a colored line in the control line region (C) tells you that you followed the test procedure properly and the proper amount of urine was absorbed.

8. What should I do if the result shows that I am not pregnant?

It means that no hCG has been detected in your urine and probably you are not pregnant. If you do not start your period within a week of its due date, repeat the test with a new test midstream. If you receive the same result after repeating the test and you still do not get your period, you should see your doctor.

PRINCIPLE

HCG Pregnancy Rapid Test Midstream is a rapid, one-step lateral flow immunoassay in midstream format for the qualitative detection of human

chorionic gonadotropin (hCG) in urine to aid in the detection of pregnancy. The test utilizes a combination of antibodies including a monoclonal hCG antibody to selectively detect elevated levels of hCG. The assay is conducted by adding urine to the hydrophil stick and obtaining the result from the colored lines

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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
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https://www.citesttestkit.com/

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