Baxter Earns CE Mark for Syringe-Infusion System Post author:Sam Post published:May 21, 2020 Post category:Devices & Diagnostics Letter The device should be available in Europe, Australia and New Zealand in June. Source: Devices & Diagnostics Letter You Might Also Like MHRA Temporarily Eases Some GMP Requirements April 23, 2020 Trump Criticizes FDA Delay of Convalescent Plasma EUA August 20, 2020 FDA Warns of Possible Failure of EpiPen Injectors March 24, 2020