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,for, Item ID-
- #1219182
- Providers like you icon 42
- LifeSign #33225-CS
Antigen Test Control Set Status™ COVID-19 / Flu A and B Positive Level / Negative Level 10 Swabs
SWAB, CONTROL SARS COV-2FLU A&B (5NEG/5POS/BX)
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Features
- Status™ COVID-19 / FLU A and B test has been granted emergency use authorization (EUA) by the FDA for use at the point-of-care setting: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
- Control Swabs for use with 1186780 (33225)
- Kit Contains: Positive Control Swab (5): Influenza A, B, and SARS-CoV-2 antigen (non-infective recombinant nucleocapsid protein) and Negative Control Swab (5): Inactivated Group B Streptococcus antigen (non-infective)
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Product Details Email
Product Specifications
| McKesson # | 1219182 |
|---|---|
| Manufacturer # | 33225-CS |
| Brand | Status™ |
| Manufacturer | LifeSign |
| Country of Origin | United States |
| Application | Control Set |
| For Use With | For Quality Control of LifeSign COVID-19 / Flu A and B Antigen Detection Test |
| HCPCS | U0002 |
| Levels | Positive Level / Negative Level |
| Product Dating | McKesson Acceptable Dating: we will ship >= 30 days |
| Test Category | Respiratory |
| Test Name | COVID-19 / Flu A and B |
| Test Type | Antigen Test |
| UNSPSC Code | 41116145 |
| Volume | 10 Swabs |
Features
- Status™ COVID-19 / FLU A and B test has been granted emergency use authorization (EUA) by the FDA for use at the point-of-care setting: https://www.fda.gov/medical-devices/emergency-situations-medical-devices/emergency-use-authorizations
- Control Swabs for use with 1186780 (33225)
- Kit Contains: Positive Control Swab (5): Influenza A, B, and SARS-CoV-2 antigen (non-infective recombinant nucleocapsid protein) and Negative Control Swab (5): Inactivated Group B Streptococcus antigen (non-infective)
- Status™ COVID-19/Flu test is a lateral flow immunoassay intended for the in vitro rapid, simultaneous qualitative detection and differentiation of nucleocapsid antigen from SARS-CoV-2, influenza A and influenza B directly from nasopharyngeal swab specimens obtained from individuals, who are suspected of respiratory viral infection consistent with COVID-19 by their healthcare provider, within the first five days of onset of symptoms
- Results are for the simultaneous identification of nucleocapsid antigens of SARS-CoV-2, influenza A and influenza B, but does not differentiate between SARS-CoV and SARS-CoV-2 viruses and is not intended to detect influenza C antigens
- Positive results indicate the presence of viral antigens, but the clinical correlation with patient history and other diagnostic information is necessary to determine infection status
- Positive results do not rule out bacterial infection or co-infection with other viruses
- Laboratories within the United States and its territories are required to report all SARS-CoV-2 results to the appropriate public health authorities
- Negative SARS-CoV-2 results should be treated as presumptive and confirmed with a molecular assay, if necessary, for patient management
- Negative results do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions
- Negative results should be considered in the context of a patient’s recent exposures, history, and the presence of clinical signs and symptoms consistent with COVID-19
- The Status™ COVID-19/Flu test is intended for use by medical professionals and laboratory personnel trained to perform the test
- Flocked swabs for superior specimen collection and patient comfort
- During the duration of the emergency this test can be performed in a patient care setting that is operating under a CUA Waiver, Certificate of Compliance or Certificate of Accreditation
More Information
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