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UK MHRA Non-Compliant Devices: DSI/2026/007 and Supply Chain Risks
The UK's MHRA has issued Device Safety Information notice DSI/2026/007, warning of non-compliant medical devices on the UK market lacking valid UKCA or CE marking. This episode breaks down the immediate actions required for healthcare providers and suppliers, such as quarantining suspect products and reporting to the MHRA. We also explore the critical implications for manufacturers, focusing on the need for enhanced post-market surveillance and rigorous supply chain oversight to prevent patient risk and ensure compliance with UK MDR 2002. Key Questions: - What is the significance of the UK…
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