Most participants indicated a preference for being introduced to the EPP after trying some ED treatments (51.0%). Participants did not have strong preference regarding the setting where they were informed about the EPP (External Penile Support Device)
ErektorFlex™ is registered by the FDA in the USA as a Class II Medical Device, with the GMDN in Europe, and with the Ministries of Health in Australia and India. Due to its effectiveness, simplicity of application, and safety, ErektorFlex™ is approved for sale without a prescription.
