This program is designed for existing BioFire^® customers who are interested in the BioFire BJI Panel (Investigational Use Only) to perform an evaluation of the product pre-FDA clearance (2.0 and Torch customers, excludes 1.5). New customers participation will be granted on a case by case basis and is restricted to 20 accounts.

Prior to submission of this form the TSM should review the program with the prospective account and notify the territory FAS and MEL. We encourage site selection of high volume orthopedic treatment centers and hospitals. If you have any questions regarding site selection, please email Jenn at jennifer.baird@biofiredx.com.

When the account has a signed contract in place, please notify your FAS for IUO software installation. When scheduling installs with your FAS please keep in mind the expected time required for initial install and training (2-3 hours). If the site is a new account requiring loaner instrumentation, be sure to include this information in your correspondence.

Note that IUO product will not be available until the end of Decemember. Once product is available, it will be sent to accounts with contracts in place and IUO software installed.

You are responsible for informing institutions that they may be subject to the Sunshine Act and obtaining any necessary information for this documentation prior to placing any order.

If there are any questions regarding this program or special needs your account may have please contact the Marketing Support Team – MarketingAssistants@biofiredx.com