In response to the urgent need for patient and caregiver safety during the COVID-19 crisis, the Emergency Relief Patient Cover exclusively serves our partners on the front lines of the pandemic.
Although the Emergency Relief Patient Cover has not been cleared or approved by the FDA, it is authorized for use by healthcare providers in contact with patients who are known or suspected to have COVID-19 under the Emergency Use Authorization for Protective Barrier Enclosures. This limited-release product helps prevent exposure to pathogenic biological airborne particulates by providing an extra barrier of protection in addition to personal protective equipment for the duration of the pandemic.†
Deployed size: 19” x 25” x 20” (W x L x H)
Stryker’s Emergency Relief Patient Cover is designed to implement an additional barrier of protection for healthcare providers and increased peace of mind.
†The product has not been FDA cleared or approved.
The product has been authorized by FDA under an EUA for use by healthcare providers (HCP) when caring for or performing medical procedures on patients who are known or suspected to have COVID-19, in healthcare settings, to prevent HCP exposure to pathogenic biological airborne particulates by providing an extra layer of barrier protection in addition to personal protective equipment.
This product is authorized only for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of medical devices, including alternative products used as medical devices, during the COVID-19 outbreak, under section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1) unless the authorization is terminated or revoked sooner.
Healthcare providers and patients, please click here to obtain healthcare provider and patient fact sheets.
Mkt Lit-1989 21 MAY 2020 REV A