Visser B.V.

Visser B.V. specializes in medical mobility solutions designed for emergency and transport vehicles. Their primary products include the Stretcher Loading System, which ensures safe patient transfer, and the Drawer Medical Work Station, which provides organized storage for medical supplies. These devices are engineered to enhance efficiency and safety in clinical and transport settings.

Visser B.V. is headquartered in the Netherlands, which means their devices are subject to EU medical device regulations. Since their products fall under EU Class I classification, they must comply with EU MDR (Medical Device Regulation) requirements, including registration in the EUDAMED database to demonstrate legal conformity and traceability.

Yes, Visser B.V.’s devices are registered in the EUDAMED database, which is the official EU portal for medical device information. This listing confirms that the devices meet EU regulatory requirements and are legally placed on the market. EUDAMED transparency helps healthcare providers, regulators, and authorities verify compliance and traceability for Class I devices.

Visser B.V.’s devices are classified as EU Class I, the lowest risk category under EU MDR. This classification means they pose minimal risk to patients and users, so they require less stringent clinical evaluation and documentation compared to higher-risk devices. However, they still must comply with essential safety and performance requirements, including proper labeling, risk management, and post-market surveillance.