Carl Martin GmbH

Carl Martin GmbH specializes in dental instruments. Their product range includes filling instruments for cavity preparation and restoration, extraction forceps for tooth removal, and technical forceps for handling dental materials. They also produce periodontal probes for measuring gum pocket depths, scalers and curettes for removing plaque and calculus, root elevators for endodontic procedures, wash-trays for sterilization, and band placers for orthodontic wire management. These devices are designed for use in dental procedures.

Carl Martin GmbH is based in Germany. Their devices are developed and manufactured in compliance with the EU Medical Device Regulation (MDR). Since all their products fall under Class I classification, they must adhere to EU regulatory requirements for active monitoring, compliance, and registration in the euDAMED database to ensure traceability and transparency.

The devices produced by Carl Martin GmbH are registered in the euDAMED database, which is the European Union’s central registry for medical devices. This registration is required for Class I devices under the EU Medical Device Regulation (MDR) to ensure they meet regulatory standards and are traceable within the EU market.

All devices manufactured by Carl Martin GmbH are classified as Class I under the EU Medical Device Regulation (MDR). This classification applies to low-risk devices like dental instruments, which typically do not require invasive procedures or carry significant health risks. Classification determines the regulatory pathway, and Class I devices must still comply with EU requirements for safety, performance, and traceability, including registration in euDAMED.