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Cardio-defib system allows for full-body MRI scans


Evera MRI ICD system is first to combine proven treatment performance, increased longevity, improved comfort with full-body MRI access.

Easily modulate, control patient temperature


Emerging medical device firm advanced cooling therapy receives European Union CE Mark for its novel esophageal cooling device

Expect Slimline Needle for use during endoscopic procedures


Innovative handle design enables physician preferences for precision, comfort, and control when acquiring tissue samples.

Plan now to comply by 2016


European medical device manufacturers face new regulations starting In 2016.

Pacemaker with event-triggered IEGM transmissions


BIOTRONIK pacemaker series offers daily automatic data transmission without relying on patient interaction

Helping to hear, again


FDA approves the first implantable hearing device for adults with a certain kind of hearing loss.

CE mark for REBEL platinum chromium coronary stent system


Newest bare metal stent technology features advanced architecture and provides physicians with enhanced treatment option for patients.

CE approval of the first 4F MR conditional lead


An ultra-thin lead, it enables access to particularly challenging vessels and offers expanded pacing options.

Endovascularly occlude blood flow in vascular abnormalities


Blockade Medical receives 510(k) clearance and CE mark of two new additions to the Barricade Coil System.

CE mark received for RENLANE system


Cordis Corp. received the European CE mark for system that treats patients suffering from resistant hypertension.

Reveal LINQ insertable cardiac monitor system


A small, wireless medical device provides long-term remote monitoring to help physicians diagnose, monitor irregular heartbeats.

CE mark for AspireSR Generator for VNS therapy


Cyberonics’ proprietary technology provides automatic stimulation upon seizure detection.

CE mark for WallFlex


Boston Scientific WallFlex esophageal fully covered metal stent provides treatment option for refractory benign esophageal strictures.

Advancing devices to treat blocked arteries in EU, US


Medtronic launches TOTAL Across Crossing Catheter in Europe and submits an application to the FDA for 510(k) clearance.

Surgical theater gets FDA clearance


Next-generation surgical theatre deliver on-demand access to real-time data and state-of-the-art imaging, during the procedure from the OR table.

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