(MENAFN- GlobeNewsWire - Nasdaq) The introduction of new Post-Market Surveillance regulations and UKCA marking processes presents key opportunities for medical device manufacturers to align compliance ...
Dublin, Jan. 28, 2026 (GLOBE NEWSWIRE) -- The "UK Conformity Assessed (UKCA) Marking for Medical Devices Training Course (Apr 15, 2026)" training has been added to ResearchAndMarkets.com's offering.
Allia Moveo combines mobility, versatility and AI-powered tools to help clinicians navigate complex minimally invasive procedures with efficiency and accuracy The Hôpital Marie-Lannelongue in France—a ...
GE HealthCare Technologies Inc. GEHC recently announced that it has obtained FDA 510(k) clearance and CE Marking for its Allia Moveo, enabling commercialization of its latest interventional imaging ...
Abbott announced it has received CE Mark in Europe for the TactiFlex Duo Ablation Catheter, Sensor Enabled to treat patients with atrial fibrillation (AFib). Following the new approval, the first ...
The company stated these findings demonstrated efficacy, safety and durability that supported the CE Mark approval. The U.S. Horizon 360 IDE study is a prospective, single-arm clinical trial ...
Medtronic plc, a global leader in healthcare technology, announced two major milestones for the Affera Sphere-360 catheter, a first-of-its-kind, all-in-one mapping and single-shot pulsed field ...
Medical Device Network on MSN
MHRA launches consultation on UK’s long-term approach to CE-marked medical devices
One of the key proposals the MHRA seeks feedback on is the ‘indefinite recognition’ of EU CE-marked medical devices in the UK.
Düsseldorf District Court issues preliminary injunction against Beijing Hanbaihan Medical Devices Co., Ltd. regarding non-CE-marked PRP tubes at MEDICA 2025 MONTHEY ...
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