A Registration Certificate is an official confirmation that a product has successfully passed state testing and registration, making it a prerequisite for legal circulation.
If you are managing a device under the ROE024RM designation, follow these steps to ensure you are current: Medical Devices - FDA roe024rm updated
: Without an updated certificate, products cannot be legally sold or used in clinical settings. A Registration Certificate is an official confirmation that
: Systems like Switzerland's swissdamed and the UK's MHRA Public Access Registration Database (PARD) have been updated to phase in mandatory device registration throughout 2025 and 2026. roe024rm updated