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Product recall for Magnificent Magnets - Gummy Bear Fridge Magnets presenting a high risk of choking.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Information about the EU Regulations and their implementation in Northern Ireland
Government funding for innovation in smart energy systems and technologies
Guidance to help you manage the security of your devices and help protect your privacy
Guidance for healthcare professionals covers the use, management and safety of in vitro diagnostic (IVD) devices, including blood glucose meters.
A government body which creates secret technologies to support national security is today launching a new drive to work more openly with technology firms and academics.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
£16.6 million investment announced today to give semiconductor researchers and businesses access to new equipment helping them test and make chips for use in high-energy machines like electric cars and manufacturing equipment.
Researchers around the world will soon be able to access millions of the natural, historic specimens found in UK museums at the click of a button as part of a £473 million UK fund to enhance key research infrastructure.
The Innovative Devices Access Pathway (IDAP) pilot is designed to accelerate the development of innovative medical devices that meet an unmet clinical need in the NHS and support their integration into the UK market.
Following a review, the MHRA has updated previous guidance (DSI/2022/003) on the use of paclitaxel coated devices (PCD) in the treatment of peripheral arterial disease (PAD).
UK guidance on re-manufacturing of Single-use medical devices.
Propose a new product for the ETL
Guidance on the procurement of in vitro diagnostic (IVD) medical devices, their safety, quality and performance.
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