United Kingdom
Intelligence de marché des dispositifs médicaux pour United Kingdom. Changements réglementaires, concurrents et tendances d'achats.
Signaux récents
The MHRA provides updated safety advice for medical device users in May 2026.
The 'Melody' paracentesis device aims to improve ascites drainage efficiency compared to standard methods.
The completed study evaluated the Creavo Vitalscan Magnetocardiograph in post-myocardial infarction patients.
Med-Tech Expo offers free registration for access to three co-located manufacturing events in Birmingham next week.
Ewa Truchanowicz discusses communication gaps in healthcare innovation at Med-Tech Expo 2026.
The Cytosponge™ device was tested for post-chemoradiation surveillance in oesophageal cancer patients in a completed study.
Signature Orthopaedics Pty Limited is registered with the FDA under code JWH, listing 2 products.
A prototype Valsalva Assist Device has completed testing in healthy volunteers to evaluate physiological responses.
A new lateral flow device test aims to quickly diagnose Aspergillosis in children at risk of invasive fungal disease.
A completed study suggests that a medical device enhancing blood flow may expedite healing in diabetic foot ulcers.
A new implantable device using micro-LEDs could enhance bladder cancer treatment effectiveness.
The UK plans tougher regulations on health self-testing kits due to safety concerns and misleading claims.
Resmed launched AirConnect Dx in the UK to enhance NHS sleep services' diagnostic capacity for OSA.
M&A and divestitures are reshaping MedTech strategies, emphasizing market access for sustained growth and valuation.
A clinical study evaluates tympanostomy tube placement using the AventaMed Solo Tympanostomy Tube Device.
Millie Marriott Webb will discuss post-single-use strategies at Med-Tech Expo 2026, focusing on MedTech advancements.
Lawrence Tallon outlines his vision for MHRA, focusing on UK medical device regulation and future leadership.
Sky Labs' blood pressure monitoring ring has received UK regulatory clearance.
LIMS is essential for ensuring GMP compliance in regulated industries like medical devices and pharmaceuticals.
Medline and Kimal issued safety notices for Namic devices, advising limited use due to disconnection and particulate risks.