New exclusive Distributor in Sweden, Denmark, Norway, Finland and Iceland.

February 15, 2026 / CMD GmbH today announced the appointment of NeoNordic ApS as exclusive distributor for Nordic Countries (Sweden, Denmark, Norway, Finland and Iceland).

NeoNordic ApS, a distributor with more than 20 years of distribution experience to the Nordic market is headquartered in Vejers Strand, Denmark and is specializes in the support and distribution of medical devices for neurosurgery market.

NeoNordic ApS will take over sales for all partners and end customers in the Nordic Countries region that were previously managed directly by CMD GmbH in Austria.

NeoNordic ApS improves support in the Nordic market and offers partners and customers maximum added value in this region.

Expansion of the strategic partnership of the sales channel in Germany, Austria, Switzerland and Luxembourg.

April 15, 2025 / CMD GmbH today announced the appointment of Chirurgische Spezialprodukte Engel (CSE) GmbH as exclusive distributor for the DACH and Luxembourg region (Germany, Austria, Switzerland and Luxembourg).

This strategic expansion represents an important step towards consolidating the long-standing partnership between CMD GmbH and Chirurgische Spezialprodukte Engel GmbH.

Chirurgische Spezialprodukte Engel GmbH, a distributor headquartered in Wadern / Germany, specializes in the support and distribution of medical devices for surgery and neurosurgery.

Chirurgische Spezialprodukte Engel GmbH will take over sales for all partners and end customers in the DACH and Luxembourg region that were previously managed directly by CMD GmbH. This creates a powerful sales channel that improves support and offers partners and customers maximum added value.

We are pleased to announce that the Skin-Elast-Hook has been successfully certified in accordance with EU Regulation 2017/745 (MDR). In addition, our quality management system has been audited and certified according to the international standard ISO 13485. In addition, our quality management system has been tested and certified in accordance with the international ISO 13485 standard.

The Skin-Elast-Hook is required for many intracranial procedures and supports safe access for the neurosurgeon.

The certifications underline our continuous commitment to the highest quality and safety standards in medical technology. The MDR certification confirms that the Skin-Elast-Hook meets all safety, performance and clinical benefit requirements as defined in the current EU regulation for medical devices. The ISO 13485 certification also proves that we operate an effective quality management system that is specifically designed for the development, production and distribution of medical products.

With these milestones, we not only create regulatory clarity, but also give our customers and partners the security of being able to rely on a tested and standard-compliant product.