Xpert® Omni-SARS-CoV-2
For emergency use under an
Emergency Use Authorization (EUA)
|
87635 |
Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]), amplified probe technique |
94500-6 |
CCI
MUE
|
$ 51.31 |
N/A
|
The HCPCS codes for High Throughput Assays (U0003 and U0005) were discontinued
EFFECTIVE FOR DATES OF SERVICE ON OR AFTER May 12, 2023 along with the PHE termination.
For more information, please see Laboratories: CMS Flexibilities to Fight COVID-19
|
Xpert® Xpress SARS-CoV-2
AND
Xpert® Xpress CoV-2 plus
For emergency use under an
Emergency Use Authorization (EUA)
|
87635-QW1 |
Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]), amplified probe technique |
94500-6 |
CCI
MUE
|
$ 51.31 |
N/A
|
Xpert® Xpress CoV-2 plus
510K - IVD.
In Vitro Diagnostic Medical Device
|
87635 |
Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]), amplified probe technique |
94500-6 |
CCI
MUE
|
$ 51.31 |
N/A
|
Xpert® Xpress CoV-2/Flu/RSV AND
Xpert® Xpress CoV-2/Flu/RSV plus
For emergency use under an
Emergency Use Authorization (EUA)
|
0241U-QW1
(all targets ordered) |
Infectious disease (viral respiratory tract infection), pathogen-specific RNA, 4 targets (severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2], influenza A, influenza B, respiratory syncytial virus [RSV]), upper respiratory specimen, each pathogen reported as detected or not detected |
95941-1
|
CCI
MUE
|
$142.63
|
N/A
|
0240U-QW1
(If only SARS CoV-2 / Flu is ordered) |
Infectious disease (viral respiratory tract infection), pathogen-specific RNA, 3 targets (severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2], influenza A, influenza B), upper respiratory specimen, each pathogen reported as detected or not detected |
95422-2
|
CCI
MUE
|
$142.63
|
N/A
|
87635-QW1
(If only SARS CoV-2 is ordered) |
Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]), amplified probe technique |
94500-6 |
CCI
MUE
|
$ 51.31 |
N/A
|
Xpert® Xpress CoV-2/Flu/RSV plus
510K - IVD.
In Vitro Diagnostic Medical Device
|
0241U
(all targets ordered) |
Infectious disease (viral respiratory tract infection), pathogen-specific RNA, 4 targets (severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2], influenza A, influenza B, respiratory syncytial virus [RSV]), upper respiratory specimen, each pathogen reported as detected or not detected |
95941-1
|
CCI
MUE
|
$142.63
|
N/A
|
0240U
(If only SARS CoV-2 / Flu is ordered) |
Infectious disease (viral respiratory tract infection), pathogen-specific RNA, 3 targets (severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2], influenza A, influenza B), upper respiratory specimen, each pathogen reported as detected or not detected |
95422-2
|
CCI
MUE
|
$142.63
|
N/A
|
87635
(If only SARS CoV-2 is ordered) |
Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (coronavirus disease [COVID-19]), amplified probe technique |
94500-6 |
CCI
MUE
|
$ 51.31 |
N/A
|
87631
(If only Flu A/B + RSV is ordered) |
Infectious agent detection by nucleic acid (DNA or RNA); respiratory virus (eg, adenovirus, influenza virus, coronavirus, metapneumovirus, parainfluenza virus, respiratory syncytial virus, rhinovirus), includes multiplex reverse transcription, when performed, and multiplex amplified probe technique, multiple types or subtypes, 3-5 targets |
85476-0
|
CCI
MUE
|
$142.63
|
N/A
|
87502
(If only Flu A/B is ordered) |
Infectious agent detection by nucleic acid (DNA or RNA); influenza virus, for multiple types or sub-types, includes multiplex reverse transcription, when performed, and multiplex amplified probe technique, first 2 types or sub-types |
92882-0
|
CCI
MUE
|
$ 95.80
|
N/A
|
The HCPCS codes for High Throughput Assays (U0003 and U0005) were discontinued
EFFECTIVE FOR DATES OF SERVICE ON OR AFTER May 12, 2023 along with the PHE termination.
For more information, please see Laboratories: CMS Flexibilities to Fight COVID-19
|