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Covid-19 POC Rapid Antibody Test Kits – Well BioTech – Box of 20 Tests

$68.80 – $86.00

Add-on: $68.80/Box

Quantity: 1 Box = 20 Individual Tests

Minimum Purchase: 1 Box

 

For use under an Emergency Use Authorization (EUA) only for the duration of the COVID-19 declaration justifying the emergency use of in vitro diagnostics (IVD) unless the EUA is terminated or revoked.

THIS IS AN ANTIBODY TEST – not suitable to diagnose a current COVID-19 infection.

This test is also authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation to test fingerstick whole blood specimens. For prescription use only.

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Specifications

 

Delivery times may be affected by product availability. New Era Industries Inc. will take reasonable steps to provide products in short supply to all customers in a timely manner. Including but not limited to separate shipments.

Description

Add-on: $68.80/Box

Quantity: 1 Box = 20 Individual Tests

Minimum Purchase: 1 Box

 

For use under an Emergency Use Authorization (EUA) only for the duration of the COVID-19 declaration justifying the emergency use of in vitro diagnostics (IVD) unless the EUA is terminated or revoked.

THIS IS AN ANTIBODY TEST – not suitable to diagnose a current COVID-19 infection.

This test is also authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation to test fingerstick whole blood specimens. For prescription use only.

Additional information

Delivery Options*

Standard Delivery, Shipped within 10 Days, Expedited Delivery, Shipped within 5 Days ( +25% )

Frequently Bought Together

Covid-19 POC Rapid Antibody Test Kits – Well BioTech – Box of 20 Tests

$68.80 – $86.00

Add-on: $68.80/Box

Quantity: 1 Box = 20 Individual Tests

Minimum Purchase: 1 Box

 

For use under an Emergency Use Authorization (EUA) only for the duration of the COVID-19 declaration justifying the emergency use of in vitro diagnostics (IVD) unless the EUA is terminated or revoked.

THIS IS AN ANTIBODY TEST – not suitable to diagnose a current COVID-19 infection.

This test is also authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation to test fingerstick whole blood specimens. For prescription use only.

Clear

SKU: N/A Category: