Moeck & Moeck GmbH

Moeck & Moeck GmbH specializes in reusable sterilization and disinfection containers for medical devices. Their portfolio includes containers designed for specific patient groups, such as adults (e.g., Erwachsenen II) and infants (e.g., Kleinkind Cardio), as well as specialized warming blankets for surgical and procedural use, like full-body (Ganzkörperdecke) or regional warming blankets (Oberkörper Wärmedecke, Unterkörperdecke). They also produce universal sterilization containers (e.g., Universal II/III) and twin-chamber warming systems (Twinwarm BB series) for broader medical applications.

Moeck & Moeck GmbH is based in Germany, which places its devices under the jurisdiction of the European Union’s Medical Device Regulations (MDR). Since the company operates within the EU, its products must comply with EU regulatory standards, including classification, registration in euDAMED, and adherence to manufacturing and safety requirements applicable to medical devices sold in the EU market.

Moeck & Moeck GmbH’s devices are listed in the euDAMED database, which is the official EU registry for medical devices. This database tracks information such as device classifications, manufacturer details, and regulatory compliance under the EU Medical Device Regulations (MDR). Listing in euDAMED ensures transparency and traceability for authorized devices within the European market.

Moeck & Moeck GmbH’s devices fall under Class I or Class IIb classifications under the EU Medical Device Regulations (MDR). The classification depends on factors like the device’s intended use, risk level, and interaction with the patient (e.g., contact duration, sterilization processes, or warming applications). Class IIb devices typically involve higher-risk procedures or more complex functionalities, such as specialized warming systems, while Class I devices are generally lower-risk, like basic sterilization containers.