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Trichomonas Vaginalis Antigen Rapid Test Kit(Immunochromatographic Assay)

    The Trichomonas vaginalis Antigen rapid test Kit is suitable for the in vitro qualitative detection of Trichomonas vaginalis antigen in swabs of vaginal secretions from women over 18 years of age for the auxiliary diagnosis of Trichomonas vaginalis infection.
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  • ICA2217-1

  • BioTeke

Warm Warning: This product is not available for US market.


A.Intended Use:
The Trichomonas vaginalis Antigen rapid test Kit is suitable for the in vitro qualitative detection of Trichomonas vaginalis antigen in swabs of vaginal secretions from women over 18 years of age for the auxiliary diagnosis of Trichomonas vaginalis infection.

B.Product details :
a. Test Specimen :Vaginal Swab
b. Sensitivity :95.36%
c. Accuracy : 97.72%
d. Specificity:99.50%
e. Reading Time : 15-20 min


C.Materials Provided :
Components: Test Card ,Sample Diluent , Sample Extraction Tube

D.Advantages :
a. Sampling is convenient and hygienic, bidding farewell to traditional urine testing and not limited to usage scenarios;
b. Higher sensitivity, pregnancy can be detected as early as 4 days before the next physiological period;
c. The results are clear and easy to understand, with a short detection time, and a positive result can be detected as soon as 20 seconds;
d.High accuracy of results.


E.Test Procedure

Please read the instruction manual seriously before testing. If the reagents in kit are stored in refrigerator, please take them out and leave them at room temperature before testing. The test should be done at room temperature. I. Specimen extraction. 

1. Put the tube into the kit box holder and gently peel off the aluminum foil seal. 

2. Insert the sampled swab into the sample diluent in the sample extraction tube, squeeze the villi part of the swab in the tube through the outer wall of the tube by finger 10 times to dissolve the potential viral antigen into solution from swab as much as possible, then remove and discard the swab. 

3. Cover the dropper lid on the sample extraction tube after step 2. 

II. Testing procedures.

1. Remove the test card by opening the aluminum foil pouch from tear notch and lay it flat. 

2. Add approximately 80μL (3 drops) of the treated specimen into the sample well of the test card. 

3. Please read the chromogenic results in the detection zone.


F.Product qualifications(By Nov.1st ,2023)


a.CE Certification - AEMPS Registration Letter
b.CE Certification - AEMPS Registration Prove
c.CE Certification - EC Declaration Of Conformity
d.CE Certification - EAR Certificate Of Notification
e.ISO 13485 Certificate
f.ISO 9001 Certificate
g.ISO 45001 Certificate
h.ISO 14001 Certificate
i.IMPS Certificate




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