Evancare Diagnostic Test Kits Vibrio Cholerae O1/O139

• Type: IVD Reagent
• Certificate: CE, ISO
• Method: Colloidal Gold Rapid Test
• Warranty: 3 Years
• Material: Medical Grade ABS Plastic
• Package: Bottle + Carton
• Model NO.: EC-CHOLERA
• Function: Early Detection
• Display: Screening
• Format: Strip+Bottle
• Name: Cholera Test Kit
• Equipment: by Eye or Machine
• Reaction Time: 5-10 Seconds
• Accuracy: 99.7%
• Delivery Time: 3-5 Days
• Temperature: 4-30 Degree
• Storage: Room Temperature
• Transport Package: Carton
• Specification: 64*50*44 cm
• Trademark: evancare or OEM
• Origin: China
• HS Code: 3002150090
• Production Capacity: 100000PCS/Day

Product Description

 

Product Description

EVANCARE Diagnostic Test Kits Vibrio cholerae O1/O139                                

 

For professional and in vitro diagnostic use only.
 

[INTENDED USE]

The Vibrio Cholerae O1 /O139 Antigen Rapid Test Cassette is a lateral flow

chromatographic immunoassay for the qualitative detection of Vibrio

Cholerae O1 /O139 antigens in human faces to aid in the diagnosis of O1/O139 group

Cholera infection.

[SUMMARY]

Cholera is an infection in the small intestine caused by the bacterium Vibrio

cholerae. The main symptoms are watery diarrhea and vomiting.

Transmission occurs primarily by drinking water or eating food that has been

contaminated by the feces (waste product) of an infected person, including

one with no apparent symptoms. The severity of the diarrhea and vomiting

can lead to rapid dehydration and electrolyte imbalance, and death in some

cases. The primary treatment is oral rehydration therapy, typically with oral

rehydration solution, to replace water and electrolytes. If this is not tolerated

or does not provide improvement fast enough, intravenous fluids can also be

used. Antibacterial drugs are beneficial in those with severe disease to

shorten.
 

The Vibrio Cholerae O1/O139 Antigen Rapid Test Cassette is a rapid test to

qualitatively detect the presence of Vibrio cholerae O1/O139 antigen in, providing

results within 15 minutes.

 

 

 

 

 

 

 

 

Detailed Photos

 

Allow the test device and specimens to reach temperature 15-30ºC

(59-86ºF) prior to testing.

1.Bring the pouch to room temperature before opening it. Remove the test

device from the sealed pouch and use it as soon as possible.

2.Place the test device on a clean and level surface.

3.Holding the specimen collection tube upright, carefully take off the tip of

collection tube, then break off the tip of collection tube, transfer 3 drops

(approximately 100 μL) to the specimen well (S) of the test device, then

start the timer. See illustration below.

4.Wait for the colored line(s) to appear. Read results at 15 minutes. Do not

interpret the result after 20 minutes.

 

Positive: *Two lines appear. One colored line should be in the control

region (C), and another apparent colored line adjacent should be in the test

region (T).

Negative: One colored line appears in the control region (C). No line

appears in the test region (T).

Invalid: Control line fails to appear. Insufficient specimen volume or

incorrect procedural techniques are the most likely reasons for control line

failure. Review the procedure and repeat the test using a new test cassette.

If the problem persists, discontinue using the lot immediately and contact

your local distributor.

 

Item No.	EVANCARE Diagnostic Test Kits Vibrio cholerae O1/O139
Contents	Each bag:1 test cassette and 1 desiccant(cassette)                  25 cassettes+25 Buffer  /box antigen test      We can put instruction as your requirement
Format / Size	Cassette:2.5mm 3.0mm 4.0mm
Methodology	Sandwich Colloidal Gold
Assay Type	Qualitative Detection
Specimen	Antigen  (fecal),
Indicator	Cholera O1/O139 Test Cassette
Storage Temperature	4-30 degree centigrade

Expiry date	3  years
Certificate	CE,ISO,FREE SALE,FDA...
Detection Limits	Home or Professional Use
Accuracy	> 99.99%
Reaction Time	3-5 min
Delivery	5-7 days
OEM Service	Available
Shipping Method	by air  or sea or international express

Company Profile

 

Certifications

 

Product Procedure

 

 

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