ARANZ Medical Achieves CE Accreditation for Silhouette under the latest European Medical Device Regulation (MDR) Standard

25 January, 2024

ARANZ Medical, a leading innovator in healthcare technology, is thrilled to announce the successful achievement of CE accreditation for its Silhouette Wound Imaging and Documentation software under the latest MDR standard. This accreditation, obtained under the European Medical Device Regulation (MDR) EU 2017/745, marks a significant milestone for the company and reaffirms its commitment to delivering cutting-edge solutions for the healthcare sector.

The CE accreditation not only validates the adherence of Silhouette to the rigorous standards set forth by the European Union for medical devices but also establishes Silhouette as a trusted and compliant solution for healthcare professionals across Europe.

The Silhouette wound imaging and documentation software operates on both Apple and Android mobile devices, giving healthcare providers easy access to advanced wound care solutions on their mobile devices. With features designed to streamline workflows and enhance accuracy, Silhouette is poised to revolutionise the way healthcare professionals manage and document wounds.

Commenting on the achievement, Dr Bruce Davey, CEO at ARANZ Medical, expressed enthusiasm, stating, “Obtaining CE accreditation for Silhouette Wound Imaging and Documentation software is a testament to our team’s unwavering commitment to excellence in healthcare technology. We are excited about the positive impact Silhouette will have on wound care management across Europe, providing healthcare professionals with powerful solutions to enhance patient outcomes.”

For more information about Silhouette Wound Imaging and Documentation software, click here.

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