Zephyr Hoverboards & Accessories - EUDAMED Registration B237ZXLATS010

Access comprehensive regulatory information for Zephyr Hoverboards & Accessories in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI B237ZXLATS010 and manufactured by Diacor Inc. in United States.

This page provides complete registration details including trade name (Zephyr Patient Positioning and Transfer System), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.