INTENDED USE
Monkeypox Virus Antigen Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of monkeypox virus antigen in human rash exudates and blood samples.

MATERIALS PROVIDED
•    Monkeypox Virus Ag Test
•    Instructions Sheet
•    Pipette
•    Swab
•    Treatment tube containing sample treatment solution
•    Buffer solution

INTENDED USE
Monkeypox Virus IgM/IgG Ab Test is a lateral flow chromatographic immunoassay used for the qualitative detection of monkeypox virus IgM and IgG antibodies in human whole blood/serum/plasma samples.

MATERIALS PROVIDED
•    Monkeypox Virus IgM/IgG Test
•    Instructions Sheet
•    Buffer solution
•    Pipette
•    Alcohol cotton
•    Sterilized lancet

INTENDED USE
Monkeypox Virus IgM/IgG Ab Test is a lateral flow chromatographic immunoassay used for the qualitative detection of monkeypox virus IgM and IgG antibodies in human whole blood/serum/plasma samples.

MATERIALS PROVIDED
•    Monkeypox Virus IgM/IgG Test
•    Instructions Sheet
•    Buffer solution
•    Pipette
•    Alcohol cotton
•    Sterilized lancet

INTENDED USE:
The saliva collection system is designed for self-contained saliva sample collection which provides critical sample consistency while amplifying, preserving, and protecting transcripts at the point of collection for highly sensitive and highly specific analysis. Sample self-collection using a saliva collection kit provides 100% in-device live viral neutralization in 10 seconds at room temperature, mitigating any risk of exposure for downstream processes. The saliva kits have no special storage or transport temperature-control requirements for collected saliva samples and eliminate the need for UN3373 biohazard shipping designation with clearance from USPS, FedEx, & UPS.

FEATURES:

• First FDA Authorized COVID-19 saliva testing solution
• First FDA Authorized at-home saliva collection device for COVID-19 testing.
• Identify infections at their earliest stage before the onset of symptoms.
• In-device 100% inactivation of the live virus within the device at ambient temps
• Maintains critical bio-sample consistency.
• 99.998% testing accuracy & more sensitive
• No temperature-controlled storage or sample transport
• Post-collection stability with no degradation in sample efficacy
• Process multiple tests from a single collected sample
• Eliminate the need for UN3373 shipping designation.
• Supported system and validated testing process.
• At-home and direct-to-patient fulfillment
• simplicity and effectiveness of saliva collection devices have delivered a new standard of care for patients and laboratories.