
MDR and Assistive Technology according to Myloc Logistics
Is your assistive technology organization in compliance with MDR? Do you and your manufacturers keep track of which of your products are classed as medical devices, including attachments and spare parts? Can your current system support identify and manage all the information required by the new law? The Medical Device Regulation (MDR) is based on international guidelines regarding product identification and aims to increase safety and especially traceability when