SRF ID : 19313007709741
Name: Mrs. SUPRIYA MARIK Registered: 06/Jun/2025 04:38PM
Age/Gender: 68
43 YY3/Female
M 10 D/Male Sample Collected: 06/Jun/2025 04:38PM
Patient ID: 132408506712 Lab Received: 06/Jun/2025 07:33PM
BarcodeNo: AA356071 Reported: 07/Jun/2025 11:10AM
Referred By: SELFSELF
DR
Nationality :Indian
MDL.
DEPARTMENT OF MOLECULAR BIOLOGY
Test Name Result Unit Biological Ref.Interval Method
SARS-CoV 2 RNA QUALITATIVE
COVID-19 RT-PCR RESULT NEGATIVE
Method: TaqMan probe Real-Time fluorescent RT-PCR.
Specimen details
Specimen: Nasopharyngeal & oropharyngeal swab. Quality of specimen on arrival: Good (in cold chain)
Interpretation of test results:
Result Interpretation
Positive Detection of RNA specific to SARS-CoV-2 (based on the CT cut-off criteria of the reaction)
Negative Not detection of RNA specific to SARS-CoV-2 within the limit of detection of the assay
Inconclusive The presence of RNA specific to SARS-CoV-2 is not certain. Repeat sampling and testing is recommended.
NOTE:
a. ICMR Registration Number for COVID-19 testing: MEDLHWB
b. The test is conducted using the kits and viral transport media (VTM) approved by ICMR/USFDA.
c. SARS-CoV-2 RT PCR test is an in vitro test for qualitative detection of Novel Corona Virus 2019 in upper respiratory tract
specimens. All results of the test should be correlated with clinical findings.
d. A single negative test result, particularly from the upper respiratory tract specimen, does not preclude Covid-19 infection.
e. A number of factors could lead to a negative result in an Covid infected individual.
1. The specimen was not handled or shipped properly.
2. Presence of mutant strain of the virus, and/or the presence of inhibitors.
3. Insufficient viral RNA in the sample.
4. Poor quality of the specimen, containing inadequate material or non representative specimen.
5. Specimen was collected late or very early during the infection.
f. Treatment of all positive cases along with contact tracing is recommended.
g. This test is recommended to use along with clinical presentations and laboratory markers (IL6, D-DIMER ) and HRCT.
h. Kindly consult referring physician / authorized hospital for appropriate follow up.
Integrated Help line - 1800-313444-222 Direct Telemedicine Line - 033-2357-6001
Ambulance Service in Kolkata for COVID-19 Patients -033-4090-2929
**End Of Report**
Checked By : BISWAJIT
SRF ID : 1931300600681
Name: Mr. SUMIT KUMAR MARIK Registered: 06/Jun/2025 04:38PM
Age/Gender: 29
43 YY3/Male
M 10 D/Male Sample Collected: 06/Jun/2025 04:38PM
Patient ID: 1324085700641 Lab Received: 06/Jun/2025 07:33PM
BarcodeNo: AA356608 Reported: 07/Jun/2025 11:10AM
Referred By: SELFSELF
DR
Nationality :Indian
MDL.
DEPARTMENT OF MOLECULAR BIOLOGY
Test Name Result Unit Biological Ref.Interval Method
SARS-CoV 2 RNA QUALITATIVE
COVID-19 RT-PCR RESULT NEGATIVE
Method: TaqMan probe Real-Time fluorescent RT-PCR.
Specimen details
Specimen: Nasopharyngeal & oropharyngeal swab. Quality of specimen on arrival: Good (in cold chain)
Interpretation of test results:
Result Interpretation
Positive Detection of RNA specific to SARS-CoV-2 (based on the CT cut-off criteria of the reaction)
Negative Not detection of RNA specific to SARS-CoV-2 within the limit of detection of the assay
Inconclusive The presence of RNA specific to SARS-CoV-2 is not certain. Repeat sampling and testing is recommended.
NOTE:
a. ICMR Registration Number for COVID-19 testing: MEDLHWB
b. The test is conducted using the kits and viral transport media (VTM) approved by ICMR/USFDA.
c. SARS-CoV-2 RT PCR test is an in vitro test for qualitative detection of Novel Corona Virus 2019 in upper respiratory tract
specimens. All results of the test should be correlated with clinical findings.
d. A single negative test result, particularly from the upper respiratory tract specimen, does not preclude Covid-19 infection.
e. A number of factors could lead to a negative result in an Covid infected individual.
1. The specimen was not handled or shipped properly.
2. Presence of mutant strain of the virus, and/or the presence of inhibitors.
3. Insufficient viral RNA in the sample.
4. Poor quality of the specimen, containing inadequate material or non representative specimen.
5. Specimen was collected late or very early during the infection.
f. Treatment of all positive cases along with contact tracing is recommended.
g. This test is recommended to use along with clinical presentations and laboratory markers (IL6, D-DIMER ) and HRCT.
h. Kindly consult referring physician / authorized hospital for appropriate follow up.
Integrated Help line - 1800-313444-222 Direct Telemedicine Line - 033-2357-6001
Ambulance Service in Kolkata for COVID-19 Patients -033-4090-2929
**End Of Report**
Checked By : BISWAJIT
