On April 14, 2020, the U.S. Food and Drug Administration granted 3B Medical Emergency Use Authorization for 3B Medical’s new High-Flow H80 System and its Luna BPAP ST non-invasive respiratory devices. These devices may now be used in the U.S. during the COVID-19 public health emergency.
“Both of these devices complement our existing line of respiratory devices. I am pleased that 3B Medical will be able to join the manufacturing industry’s collective surge in production capacity to meet global shortages across the board for all therapeutic devices used to treat COVID-19 patients” said Jose Llana, M.D., 3B Medical’s Vice President of Sales.
Source: 3B Medical
