SOFTNETA is proud to announce that from the 7.8.1 version MedDream DICOM Viewer is FDA cleared K222320 for diagnostic use including mammographic images!

Read more about FDA 510(k) clearance for MedDream as a Class II medical device.

MedDream also supports IHE (XDS-I.b) profile, is CE Class IIb certified, registered in United Kingdom, Switzerland,  and more. Read more about all MedDream registrations and certifications here.

Read more about MedDream DICOM Viewer.