FCoV + FPV + Giardia Lamblia Antigen Combo Rapid Test Cassette Feces Specimen

Application

PRINCIPLE

FCoV+FPV+Giardia Lamblia Antigen Combo Rapid Test Cassette is based on sandwich lateral flow immunochromatographic assay. The test device has three testing windows. Each testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample well on the cassette, the liquid will laterally flow on the surface of the test strip.

If there is enough FCoV or FPV or Giardia antigen in the sample, a visible T line will appear in the corresponding testing window. The C line should always appear after a sample is applied, indicating a valid result. By this means, the cassette can accurately indicate the presence of FCoV or FPV or Giardia antigen in the sample.

PRECAUTIONS

Do not use after expiration date.

Handle all specimens as if they contain infectious agents. Observe established precautions against microbiological hazards throughout testing and follow the standard procedures for proper disposal of specimens.

Wear disposable gloves and eye protection when specimens are being tested.

Humidity and temperature can adversely affect results.

Do not remove test cassette from its pouch until immediately before use.

Do not reuse the test kit.

Do not mix components from different lot and different products.

DIRECTIONS FOR USE

Allow the test cassette, specimen, buffer, and/or controls to equilibrate to room temperature (15-30 °C) prior to testing.

1.Collect feces with the swab stick from anus or from the ground. The amount of fecal swab as follows:

2.Insert the wet swab into the buffer tube provided with the kit. Swirl and shake to ensure sufficient sample extraction.

3.Place the test cassette on a clean and level surface. Hold the dropper vertically and transfer 4 drops of extracted sample (approximately 160 μl) to each specimen well (S) of the test cassette, then start the timer. See illustration above.

4.Read the result in 10 minutes. Do not interpret results after 15 minutes.

INTERPRETATION OF RESULTS

Positive: The presence of both C line and T line, regardless of T line being strong or faint.

Negative: Only clear C line appears.

Invalid: No colored line appears in C region, regardless of T line’s appearance

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 manufactures its IVD products in ISO13485:2016 accredited manufacturing facilities under strict quality assurance systems. Our innovative products are developed using industry-leading design control systems, which ensures consistent product quality and performance.

Our products are used in the clinical market to help people live more healthy lives. When you select CITEST products, you can be assured of high performance and accuracy along with a dedicated customer support team.