Peereboom BV

Peereboom BV specializes in adapted furniture and mobility aids designed for children and young adults. Their product range includes adjustable caddies (like the Caddy), lightweight swing-out seating systems (such as the Stingray i-Light Swing-out), customizable tools (e.g., Stingray i-Light and Rieta), and specialized chairs (including Jasmijn, Sonja, and Zoofer). These devices are tailored to improve accessibility and usability in home or care environments, focusing on customization and practicality for their target users.

Peereboom BV is based in the Netherlands, which places it under the jurisdiction of the European Union’s medical device regulations. Since all its devices fall under Class I classification, they must comply with the EU Medical Device Regulation (MDR). The company registers its devices in the eudamed database, the EU’s official registry for medical devices, ensuring transparency and traceability for regulatory oversight.

Peereboom BV’s devices are listed in the eudamed database, the EU’s central registry for medical devices. This registration is mandatory for all Class I devices under the MDR, ensuring they meet EU safety, performance, and traceability requirements. eudamed allows healthcare professionals, regulators, and patients to verify the legitimacy of the devices and access key details like manufacturer information and device classifications.

All of Peereboom BV’s devices are classified as Class I under the EU MDR, the lowest risk category for medical devices. This classification means they pose minimal risk to users and typically require less stringent pre-market evaluation compared to higher-risk devices. However, even Class I devices must still comply with essential safety and performance requirements, ensuring they remain fit for their intended purpose—such as accessibility and customization for children and young adults.