All CareStart™ products from AccessBio are manufactured in the U.S. and distributed by Blue Wave Medical, a U.S. company headquartered in California.
CareStartTM COVID-19 Antigen Point-of-Care Tests are authorized under EUA.
AccessBio is a global pioneer in invitro diagnostic technologies. AccessBio works with the World Health Organization, UNICEF and other global initiatives.
On July 16, 2021, FDA granted an extension of the shelf-life of CareStartTM COVID-19 Antigen Point-of-Care tests when stored at 1-30*C.
Accordingly, certain CareStartTM COVID-19 Antigen Point-of-Care tests that are currently labeled with expiration dates between February 2021 and November 2021 in fact have longer shelf lives than indicated by the expiration date on the label. A copy of FDA’s letter to Access Bio regarding the shelf-life extension is available at the following link: https://www.fda.gov/media/150840/download.
Our customers are important to us. Let us know how we can help you.
This test is authorized for use at the Point of Care (POC), i.e., inpatient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.
To request a quote for specific quantity, click the link for Care State POC https://forms.gle/dHuxzCznh9QEtxvb7 or click the link for On/Go OTC https://forms.gle/LB4ydmF1vwpvCyLv7.
Open today | 09:00 am – 05:00 pm |
Copyright © 2022 Blue Wave Medical - All Rights Reserved.
This test is authorized for use at the Point of Care (POC), i.e., inpatient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.
All purchases require a copy of your Sellers Permit, Resale Certificate and CLIA Certificate of Waiver to process the order.