Moritz Reha-Hilfen GmbH

Moritz Reha-Hilfen GmbH specializes in pressure-relief and positioning aids, including cushions and supports for medical use. Their product range covers items like wedge-shaped pillows (e.g., Refluxkissen, Positurkissen) for spinal alignment and reflux management, as well as contoured and segmented foam supports (e.g., Spitzfuß-Lagerungskissen, Keilkissen) for foot and leg positioning. These devices are designed to enhance patient comfort and support in clinical or homecare settings, focusing on non-invasive, low-risk applications.

The company is headquartered in Germany and manufactures devices that fall under the EU’s Class I medical device classification. This classification applies to low-risk, non-invasive products like their cushions and positioning supports, which are intended for patient comfort and minor anatomical support. As such, their devices must comply with EU medical device regulations, including registration in the eudamed database.

Yes, all of Moritz Reha-Hilfen GmbH’s devices are registered in the eudamed database, which is the official EU registry for medical devices. This registration is required for Class I devices under EU medical device legislation, ensuring transparency and traceability for healthcare providers and regulatory authorities.

Moritz Reha-Hilfen GmbH’s devices are classified as EU Class I medical devices. This classification is determined by their intended use—primarily as non-invasive, low-risk products for patient positioning, pressure relief, and comfort. Class I devices typically require basic conformity assessments and registration but do not undergo rigorous clinical trials, as they pose minimal risk to patients.