The SARS-CoV-2 Coronavirus pandemic has created unprecedented challenges for patient care and staff safety. To provide an immediate, short term solution to the shortage of Personal Protective Equipment (PPE), STERIS is pleased to announce the following:
The FDA has granted STERIS an Emergency Use Authorization (EUA). This allows STERIS to temporarily provide a distinct option to effectively decontaminate compatible N95 or N95-equivalent Respirators up to 10-times using the Non-Lumen Cycle of the V-PRO® Low Temperature Sterilization System (Models: 1 Plus, maX and maX 2).
Use the resources below to help navigate through the Emergency Use Authorization.
If you have specific questions, please contact your STERIS Account Manager, Clinical Specialist and/or submit your questions using the Contact Us link below:
