Viral Transport Medium Inactivated Biochemistry Test Kit For RT-PCR

Viral Transport Medium (Inactivated Type), Suitable for RT-PCR, Viral Transport Medium

The Viral Transport Medium is intended for the collection and transport of clinical samples containing viruses, chlamydiae, mycoplasmas and ureaplasmas from the collection site to the testing laboratory.

PRODUCT FEATURES

Directly lyse the virus and release nucleic acid

Suitable for RT-PCR

Quickly inactivate the virus

Eliminate the risk of infection

[Preservation]

Storage: 5-25℃ Expiration date: 12 months
Please refer to the outer box for the production date and expiration date.

[Sample Requirements]
The collected nasopharyngeal swab samples should be transported at 2°C-8°C and submitted for inspection immediately. Sample transport and storage time should be no later than 48h.

[Testing method]

1. Before sampling, mark the relevant sample information on the label of the sampling tube.
2. Use a sampling swab to sample at the nasopharynx up to different sampling requirements.
3. Sampling methods are below:
a. Nasal swab: Gently insert the swab head into the nasal condyle of the nasal passage, stay for a while and then slowly turn it out. Wipe the other nostril with another swab, immerse the swab head in the sampling solution, and discard the tail.
b. Pharyngeal swab: Wipe the bilateral pharyngeal tonsils and posterior pharyngeal wall with the swab, immerse the swab head in the sampling solution, and discard the tail.
4. Quickly place the swab into the sampling tube.
5. Break the sampling swab above the sampling tube, and tighten the tube cap.
6. Freshly collected clinical specimens should be delivered to the laboratory within 2 hours at 2°C-8°C.

[Interpretation of results]

If the collected sampling solution turns yellow or turbid, the sample should be re-sampled for testing.

[Method limitations]

1. Contaminated samples after collection will affect the final results.

2. Store samples at inappropriate temperature will affect the final results.

Advantages:

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.