
Respiratory Test Kit Lucira COVID-19 and Flu Home Test 1 Test per Kit
- Lucira by Pfizer COVID-19 & Flu Home Test has not been FDA cleared or approved but has been authorized for emergency use by FDA under an Emergency Use Authorization (EUA):
- The Lucira by Pfizer COVID-19 & Flu Home Test is a single use (disposable) home test kit intended for simultaneous rapid in vitro qualitative detection and differentiation of SARS-CoV-2, influenza A, and influenza B viral nucleic acid
- This test is authorized for non-prescription home use with anterior nasal swab samples from individuals 14 years or older (self-collected) or individuals 2 years or older (collected by an adult) with signs and symptoms consistent with a respiratory tract infection, including COVID-19
- Positive results indicate the presence of viral nucleic acid, but clinical correlation with past medical history and other diagnostic information is necessary to determine infection status
- Positive results do not rule out bacterial infection or co-infection with other pathogens not detected by the test
- Negative results for SARS-CoV-2 and influenza B are presumptive, meaning that they should be confirmed, if necessary for patient management, with an authorized or cleared molecular test performed in a CLIA-certified laboratory that meets requirements to perform high or moderate complexity tests
- Negative results do not rule out SARS-CoV-2, influenza A, and/or influenza B infection and should not be used as the sole basis for treatment or other management decisions, including infection control decisions
- This Lucira by Pfzer COVID-19 & Flu Home Test contains everything needed to perform one (1) Lucira by Pfzer COVID-19 & Flu Home Test: Instructions, 2 AA Batteries, 1 test unit, 1 sample vial, 1 sterile nasal swab and 1 disposal bag
Product Specs
| Item Number | 1259231 |
|---|---|
| Catalog Number | 0069-9701-48 |
| UOM | CS |
| Level 1 Family Description | Lab-Waived Lab |
| Level 2 Category Description | Lab-Respiratory Testing |
| Level 3 Group Description | Combo Tests |
| Level 4 Sub-Category Description | Flu-COVID Molecular Testing |
| Application | Respiratory Test Kit |
| Brand | Lucira |
| Buy American Act (BAA) Compliant | No |
| Contents 1 | Each Kit contains: (1) Test Unit, (1) Sample Vial, (1) Sterile Nasal Swab, (1) Disposable Bag, (2) AA Batteries, Instructions |
| Country of Origin | Unknown |
| FSA Eligible - Buy UOM | Yes |
| FSA Eligible - Primary UOM | Yes |
| FSA Eligible - Sell UOM | Yes |
| Manufacturer | Pfizer (Lab) |
| Manufacturer # | 0069-9701-48 |
| McKesson # | 1259231 |
| Number of Tests | 1 Test per Kit |
| Purchase Program Type | Standard Purchase |
| Reading Type | Visual Read |
| Sample Type | Anterior Nasal Swab Sample |
| Specialty | Molecular |
| Test Format | Test Device Format |
| Test Kit Type | Rapid |
| Test Name | COVID-19 and Flu Home Test |
| Test Type | Nucleic Acid Amplification Test (NAAT) |
| Time to Results | 30 Minute Results |
| Trade Agreement Act (TAA) Compliant | No |
| UNSPSC Code | 41116144 |
- Lucira by Pfizer COVID-19 & Flu Home Test has not been FDA cleared or approved but has been authorized for emergency use by FDA under an Emergency Use Authorization (EUA):
- The Lucira by Pfizer COVID-19 & Flu Home Test is a single use (disposable) home test kit intended for simultaneous rapid in vitro qualitative detection and differentiation of SARS-CoV-2, influenza A, and influenza B viral nucleic acid
- This test is authorized for non-prescription home use with anterior nasal swab samples from individuals 14 years or older (self-collected) or individuals 2 years or older (collected by an adult) with signs and symptoms consistent with a respiratory tract infection, including COVID-19
- Positive results indicate the presence of viral nucleic acid, but clinical correlation with past medical history and other diagnostic information is necessary to determine infection status
- Positive results do not rule out bacterial infection or co-infection with other pathogens not detected by the test
- Negative results for SARS-CoV-2 and influenza B are presumptive, meaning that they should be confirmed, if necessary for patient management, with an authorized or cleared molecular test performed in a CLIA-certified laboratory that meets requirements to perform high or moderate complexity tests
- Negative results do not rule out SARS-CoV-2, influenza A, and/or influenza B infection and should not be used as the sole basis for treatment or other management decisions, including infection control decisions
- This Lucira by Pfzer COVID-19 & Flu Home Test contains everything needed to perform one (1) Lucira by Pfzer COVID-19 & Flu Home Test: Instructions, 2 AA Batteries, 1 test unit, 1 sample vial, 1 sterile nasal swab and 1 disposal bag
Product Specs
| Item Number | 1259231 |
|---|---|
| Catalog Number | 0069-9701-48 |
| UOM | CS |
| Level 1 Family Description | Lab-Waived Lab |
| Level 2 Category Description | Lab-Respiratory Testing |
| Level 3 Group Description | Combo Tests |
| Level 4 Sub-Category Description | Flu-COVID Molecular Testing |
| Application | Respiratory Test Kit |
| Brand | Lucira |
| Buy American Act (BAA) Compliant | No |
| Contents 1 | Each Kit contains: (1) Test Unit, (1) Sample Vial, (1) Sterile Nasal Swab, (1) Disposable Bag, (2) AA Batteries, Instructions |
| Country of Origin | Unknown |
| FSA Eligible - Buy UOM | Yes |
| FSA Eligible - Primary UOM | Yes |
| FSA Eligible - Sell UOM | Yes |
| Manufacturer | Pfizer (Lab) |
| Manufacturer # | 0069-9701-48 |
| McKesson # | 1259231 |
| Number of Tests | 1 Test per Kit |
| Purchase Program Type | Standard Purchase |
| Reading Type | Visual Read |
| Sample Type | Anterior Nasal Swab Sample |
| Specialty | Molecular |
| Test Format | Test Device Format |
| Test Kit Type | Rapid |
| Test Name | COVID-19 and Flu Home Test |
| Test Type | Nucleic Acid Amplification Test (NAAT) |
| Time to Results | 30 Minute Results |
| Trade Agreement Act (TAA) Compliant | No |
| UNSPSC Code | 41116144 |
Original: $1,253.35
-65%$1,253.35
$438.67Description
- Lucira by Pfizer COVID-19 & Flu Home Test has not been FDA cleared or approved but has been authorized for emergency use by FDA under an Emergency Use Authorization (EUA):
- The Lucira by Pfizer COVID-19 & Flu Home Test is a single use (disposable) home test kit intended for simultaneous rapid in vitro qualitative detection and differentiation of SARS-CoV-2, influenza A, and influenza B viral nucleic acid
- This test is authorized for non-prescription home use with anterior nasal swab samples from individuals 14 years or older (self-collected) or individuals 2 years or older (collected by an adult) with signs and symptoms consistent with a respiratory tract infection, including COVID-19
- Positive results indicate the presence of viral nucleic acid, but clinical correlation with past medical history and other diagnostic information is necessary to determine infection status
- Positive results do not rule out bacterial infection or co-infection with other pathogens not detected by the test
- Negative results for SARS-CoV-2 and influenza B are presumptive, meaning that they should be confirmed, if necessary for patient management, with an authorized or cleared molecular test performed in a CLIA-certified laboratory that meets requirements to perform high or moderate complexity tests
- Negative results do not rule out SARS-CoV-2, influenza A, and/or influenza B infection and should not be used as the sole basis for treatment or other management decisions, including infection control decisions
- This Lucira by Pfzer COVID-19 & Flu Home Test contains everything needed to perform one (1) Lucira by Pfzer COVID-19 & Flu Home Test: Instructions, 2 AA Batteries, 1 test unit, 1 sample vial, 1 sterile nasal swab and 1 disposal bag
Product Specs
| Item Number | 1259231 |
|---|---|
| Catalog Number | 0069-9701-48 |
| UOM | CS |
| Level 1 Family Description | Lab-Waived Lab |
| Level 2 Category Description | Lab-Respiratory Testing |
| Level 3 Group Description | Combo Tests |
| Level 4 Sub-Category Description | Flu-COVID Molecular Testing |
| Application | Respiratory Test Kit |
| Brand | Lucira |
| Buy American Act (BAA) Compliant | No |
| Contents 1 | Each Kit contains: (1) Test Unit, (1) Sample Vial, (1) Sterile Nasal Swab, (1) Disposable Bag, (2) AA Batteries, Instructions |
| Country of Origin | Unknown |
| FSA Eligible - Buy UOM | Yes |
| FSA Eligible - Primary UOM | Yes |
| FSA Eligible - Sell UOM | Yes |
| Manufacturer | Pfizer (Lab) |
| Manufacturer # | 0069-9701-48 |
| McKesson # | 1259231 |
| Number of Tests | 1 Test per Kit |
| Purchase Program Type | Standard Purchase |
| Reading Type | Visual Read |
| Sample Type | Anterior Nasal Swab Sample |
| Specialty | Molecular |
| Test Format | Test Device Format |
| Test Kit Type | Rapid |
| Test Name | COVID-19 and Flu Home Test |
| Test Type | Nucleic Acid Amplification Test (NAAT) |
| Time to Results | 30 Minute Results |
| Trade Agreement Act (TAA) Compliant | No |
| UNSPSC Code | 41116144 |



