MedDream is Registered in Russia




HTML5 Dicom viewer MedDream registered in Russia

We are proud to announce that Federal Service for Surveillance in Healthcare (Roszdravnadzor), a federal executive body responsible for control and supervision of the Healthcare system, has registered medical software MedDream as class 2b medical device.

Press here to see registration documentation.

MedDream is also FDA cleared K162011 as a class II medical device and CE class IIa certified.

Read more about MedDream DICOM Viewer certifications here.