090-70-0071

SARS-CoV-2 Real-time RT-PCR

In case of walk-in patient, please make the appointment for patient first, call 02-011-5566

Nasopharyngeal swab and throat swab/ Transport medium 3 ml, 1 tube

Nasopharyngeal swab and throat swab/ Transport medium 3 ml, 1 tube

Transport medium

at 2-8°C for up to 5 days

090-70-0071

SARS-CoV-2 Real-time RT-PCR

Real-Time Fluorescent RT-PCR

24 hours service 

Specimen received to reported 2 hours

Molecular biology & Genetics, Laboratory Department Tel.14168

5 days

090-70-0071

SARS-CoV-2 Real-time RT-PCR

Acute respiratory infection can be caused by a variety of viruses and bacteria, including recently introduced SARS-CoV-2. Acute respiratory infection of SARS-CoV-2 outbreak in Wuhan, China has widely spread out into the world since 2019. Common signs of a person infected with SARS-CoV-2 include respiratory symptoms, fever, cough, shortness of breath, and dyspnea. In more severe cases, the infection generates pneumonia, acute respiratory syndrome, kidney failure, or even death. 

Not Detected

1. This test is supportive for the diagnosis of SARS-CoV-2 infection. The test results are only for clinical reference only. The clinical diagnosis and treatment of patients should be combined with their symptoms and signs, medical history, other laboratory tests and treatment responses considering
2. Erroneous test results might occur from improper specimen collection, failure to follow the recommended sample collection, handling and storage procedures, technical error, sample mix-up, or because the number of organisms in the specimen is too low to be detected by the test. 
3. Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for treatment or other patient management decisions.
4. Viral nucleic acid may persist in vivo, independent of virus viability. Detection of analyte target(s) does not imply that the corresponding virus(es) are infectious or are the causative agents for clinical symptoms.
5. Mutations within the target regions of the M10 SARS-CoV-2 test could affect primer and/or probe binding resulting in failure to detect the presence of virus or the virus being detected less predictably.
6. The test is specific for SARS-CoV-2 therefore, the results do not exclude the possibility of infection with other respiratory viruses or bacterial infection.

Manufacturer’s packages insert, STANDARD™ M10 SARS-CoV-2, December 2022, SD Biosensor Inc, Chungcheongbuk-do 28161, Korea.