Professional Manufacturer of Rapid Test Devices
|Place of Origin:||China|
|Certification:||ISO9001, CE, TUV, FDA|
|Model Number:||TP (Treponema Pallidum) Syphilis|
|Minimum Order Quantity:||10 Boxes or 400 Kits (40 Kits/Box)|
|Price:||Negotiable as per Order Quantity|
|Packaging Details:||40 Kits/Box, 50 Boxes/Carton, 317g/Box, 18kgs/Carton, Box Size: 250x125x65mm, Carton Size: 650x510x330mm|
|Delivery Time:||8 days|
|Payment Terms:||T/T, Western Union, MoneyGram|
|Supply Ability:||100,000 Kits Per Day|
|Shelf Life:||2 Years||Format:||Cassette|
|OEM / ODM:||Available||Result Time:||Read In 20 Minutes|
|Usage:||For In Vitro Diagnostic Use Only||Box Color:||Blue|
Treponema Pallidum Screening Test Kit,
IVD Syphilis Rapid Test Kit,
Treponema Pallidum Rapid Test Kit
Treponema Pallidum(TP) Rapid Diagnostic Kit (Colloidal Gold)
For the Qualitative Detection of Syphilis Antibodies in serum/plasma and whole Blood
☀ High Sensitivity
☀ High Specificity
☀ Reliable: Accuracy higher than 97.5%, early detection of the presence of TP Antibody
☀ Convenient: Room Temperature Storage, Built-In Control
☀ Simple: No Instrument Required
☀ Fast: Results in 5-30 minutes, strong positive results may be observed promptly within 3 minutes
☀ Certified by Authoritative Certification System and Standards
☀ Winner of "the National Rapid Diagnostic Kit for Clinical Performance Assessment"
The Syphilis Rapid Diagnostic Test is a qualitative test for the detection of antibodies to Syphilis in human serum/plasma and whole blood. It is considered as an initial screening test for Syphilis antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA.
Reagents and Materials Provided
☀ Blood diluent in a dropper bottle.
☀ One sealed pouched cassette with desiccant & a disposable pipe.
☀ One piece of operating instruction with 40 test pouches.
Sample Collection and Preparation
Whole Blood ( Finger stick Specimens)
☀ Clean the area to be lanced with an alcohol swab.
☀ Squeeze the end of the fingertip and pierce it with a sterile lancet.
☀ Wipe away the first drop of blood with sterile gauze or cotton.
☀ Allow the second drop to flow directly into a sample well.
☀ Have a certified phlebotomist collect whole blood into a purple, blue or green top collection tube (containing EDTA, citrate or heparin, respectively) by veinpuncture.
☀ Separate the plasma by centrifugation.
☀ Carefully withdraw the plasma for testing or label and store it at 4°C for up to five days. Plasma may be frozen at -20°C for at least three months.
☀ Have a certified phlebotomist collect whole blood into a red top collection tube (containing no anticoagulants) by veinpuncture.
☀ Allow the blood to clot.
☀ Separate the serum by centrifugation.
☀ Carefully withdraw the serum for testing or label and store it at 4°C for up to five days. Serum may be frozen at -20°C for at least three months.
Store the test kits at temperature 4-30°C,in the sealed pouch for the duration of the shelf life (24 months).
Interpretation of Results
Negative:No apparent band in the test region (T), Only one red band appears in the control region (C). This indicates that no TP antibodies have been detected.
Positive: In addition to one red band in the control region (C), a red band will appear in the test region (T). This indicates that the specimen contains TP antibodies.
Invalid: If no band appears in the control region(C), regardless of the presence or absence of band in the test region (T). It indicates a possible error in performing the test. The test should be repeated using a new device.
Serum or Plasma Sample
Add 2 drops of serum or plasma into sample well. Observe the result in 120 minutes.
Whole Blood Sample
Add 1 drop of whole blood into sample well, after all blood completely absorbed. Add 2 drop of whole blood diluent. Observe the result in 20 minutes.
Warning and Precautions
☀ FOR IN VITRO DIAGNOSTIC USES ONLY.
☀ All patient samples should be treated as if capable of transmitting diseases.
☀ Do not interchange reagents from different lots or use test kit beyond expiration date.
☀ Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results.
Within run and between run precisions have been determined by testing 10 replicates with three of the samples: a negative, a weak positive, and a strong positive sample. The negative, weaker positive, and strong positive samples were correctly identified in all of the tests every time.
Contact Person: Mr. Randy.Zhang