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One Step FFN Home Fertility Testing Kits High Accuracy Visually Interpreted

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China Orient New Life Medical Co.,Ltd. certification
We are satisfied with your quality & services so far. The HIV 1/2 antibody Test performance is perfect.

—— Katrina

I have to say that New Life provides high quality products. The FOB, Troponin I, HIV, HCV, Drug Abuse test all performed very well in our market.

—— Clemen

Your Dengue IgG/IgM and Malaria test perfromed well. Now we want to try your Filariasis test in our market.

—— Primo

One Step FFN Home Fertility Testing Kits High Accuracy Visually Interpreted

One Step FFN Home Fertility Testing Kits High Accuracy Visually Interpreted
One Step FFN Home Fertility Testing Kits High Accuracy Visually Interpreted One Step FFN Home Fertility Testing Kits High Accuracy Visually Interpreted

Large Image :  One Step FFN Home Fertility Testing Kits High Accuracy Visually Interpreted Get Best Price

Product Details:
Place of Origin: China
Brand Name: New Life
Certification: ISO13485, CE,FDA
Model Number: Strip
Payment & Shipping Terms:
Minimum Order Quantity: 5000pcs
Packaging Details: 1pc/pouch, 25pcs/box
Delivery Time: 20-30days
Payment Terms: T/T, Western Union
Supply Ability: 2000000pcs/month
Detailed Product Description
Category: Fertility Format: Multiple
Specimen: Urine Testing Time: 5-15 Minutes
Shelf Life: 24 Months Detection: FFN
Accuracy: 98.68%
High Light:

female fertility test kit

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reliable pregnancy test kit

One Step fetal fibronectin (fFN) rapid test, Home fertility testing kits, high accuracy

 

 

INTENDED USE:

 

The fetal fibronectin (fFN) rapid test (vaginal secretion) is a visually interpreted, qualitative immunochromatographic test device for detection of fFN in vaginal secretions during pregnancy, which is a special protein that literally holds your baby in place in the womb. The test is intended for professional use to help diagnose the rupture of fetal membranes (ROM) in pregnant women.

 

 

TEST PRINCIPLE

 

The fFN (vaginal secretion) has been designed to detect fFN thrisough visual interpretation of color development in the internal Device. The membrane was immobilized with anti-fFN antibodies on the test region. During the test, the specimen is allowed to react with colored anti-fFN antibodies colloidal gold conjugates, which were precoated on the sample pad of the test. The mixture then moves on the membrane by a capillary action, and interact with reagents on the membrane. If there were enough fFN in specimens, a colored band will form at the T region of the membrane. Presence of colored band indicates a positive result, while its absence indicates a negative result. Appearance of a colored band at the control region serves as a procedural control. This indicates that proper volume of specimen has been added and membrane wicking has occurred.

 

 

TEST PROCEDURE


1.  Remove the test from its sealed pouch, and place it on a clean, level surface. Label the test with patient or control identification. To obtain a best result, the assay should be performed within one hour.

2.  Insert the swab into the specimen tube containing 1ml of assay diluent.

3.  add the Vaginal secretion into the specimen tube containing 1000ml of assay diluent using the dropper.

4.  Mix the swab samples with assay diluent to extract well.

5.  Hold the dropper vertically and transfer 3 full drops of specimen (approx. 100 uL) to the specimen well (S) of the test device, and then start the timer. Avoid trapping air bubbles in the specimen well (S).

6.  Wait for the colored band to appear. The result should be read at 10 minutes. Do not interpret the result after 20 minutes.

 

 

INTERPRETATION OF RESULTS

 

 

POSITIVE: Two distinct colored lines are visible, and the line in the test line region (T) is the same as or darker than the line in the control line region (C). A positive result indicates that the FSH level is higher than normal and the subject may be experiencing perimenopause.

 

NEGATIVE: Two colored 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 indicates that the subject is probably not experiencing perimenopause in this cycle.

 

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

 

 

Kit Components

 

 

Individually packed test Devices Each Device contains colored conjugates and reactive reagents pre-spreaded at the corresponding regions.
Specimens collection swab For specimens collection use.
Specimens dilution tube with buffer 0.1 M Phosphate buffered saline (PBS) and preservative
Package insert For operation instruction.
   

 

 

NOTE: 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 device. If the problem persists, please contact your local distributor.

 

ORIENT NEW LIFE MEDICAL CO., LTD.
Contact: Jerry Meng
Email: Jerry @ newlifebiotest .com
Tel. +86 18657312116
SKYPE enetjerry

Contact Details
Orient New Life Medical Co.,Ltd.

Contact Person: Jerry Meng

Tel: +8618657312116

Send your inquiry directly to us