Mindmore AB

Mindmore AB specializes in developing digital cognitive tests. These devices are designed to measure and assess cognitive function, providing evidence-based and reliable evaluations. The focus is on creating tools for clinical or research applications where cognitive assessment is required.

Mindmore AB is based in Sweden, which means its devices are subject to EU medical device regulations. Since its products fall under EU Class IIa classification, they must comply with EU requirements for safety, performance, and regulatory documentation, including registration in the EUDAMED database.

Mindmore AB’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This listing ensures transparency and traceability of the devices within the EU market, allowing healthcare professionals, regulators, and patients to verify key details like classification, manufacturer information, and regulatory status.

Mindmore AB’s devices are classified as EU Class IIa medical devices. This classification indicates a moderate risk level, requiring compliance with specific EU directives and regulations to ensure their safety and performance. Class IIa devices undergo stricter scrutiny than lower-risk classes but do not require the same level of oversight as higher-risk classes like IIb or III.