Medtronic’s Arctic Front Advance™ Cryoablation System now delivers cold therapy to a larger area more evenly, the company claiming that this will aid cardiologists in delivering cardiac ablation therapy.
CE Mark Approval
CE Mark For Cerbomed’s Transcutaneous Vagus Nerve Stimulation Pain Relief Indication
Germans medical device company Cerbomed GmbH has received CE mark clearance for the application of transcutaneous Vagus Nerve Stimulation (t-VNS) in pain relief therapy.
Medtronic’s Newly CE Marked Cardiac Resynchronisation Therapy Devices Preserve Normal Heart Rhythm
Medtronic has announced CE mark approval for two new CRT devices which automatically adapt to patients’ electrical rhythms, improving response to life-saving therapy.
CE Mark And EU Launch For Abbott’s XIENCE Xpedition™ “Extraordinarily Deliverable” Drug Stent
Abbott has announced that the XIENCE Xpedition™ Everolimus Eluting Coronary Stent System has gained CE Mark approval for the treatment of coronary artery disease. The company is launching the product immediately in CE Mark countries.
Attrius® Cardiac PET System Gains CE Mark
Based out of Shenyang, China, Neusoft Positron Medical Systems, a joint venture between Neusoft Medical Systems Co., Ltd., and Positron Corporation has received ISO certification (9001:2008 & 13485:2003) and CE Mark approval for the Attrius® PET Systems.
CE Mark Means EndoStim LES Stimulator Is Now A treatment Option In Gastro-esophageal Reflux Disease
EndoStim B.V. has announced CE Mark approval of its LES Stimulation System for the treatment of gastro-esophageal reflux disease (GERD). The system uses low energy electrical pulses to strengthen a weak or dysfunctional lower esophageal sphincter muscle.
CE Mark for Gore’s Hybrid Vascular Graft Signals Preservation Of Dialysis Access Sites
W L Gore’s Hybrod Vascular Graft was FDA cleared two years ago, and now the company has announced it has its CE Mark, which it expects will bring a new level of utility to Vascular Surgeons in Europe.
CE Mark For Teleflex’s Newly Acquired Vascular Access Catheter
Teleflex Incorporated has announced that its Semprus BioSciences subsidiary has gained CE mark for its Nylus™ Peripherally Inserted Central Catheter with Semprus Sustain™ technology.
CE Mark For Boston Sci’s MRI Compatible Pacemakers
Boston Scientific Corporation has received CE Mark approval for use of its MRI compatible INGENIO™ and ADVANTIO™ pacemakers
CE Mark For Sunshine Heart’s C-Pulse® Heart Assist System
Sunshine Heart, Inc. has received CE Mark approval for its C-Pulse Heart Assist System for the treatment of Class III and ambulatory Class IV heart failure.
CE Mark For Lazarus Effect Funnel™ Guide Catheter
Nice product, well done for the CE Mark, but should Lazarus Effect be issuing a press release when it’s website’s not even finished? As medtech marketers we’re stumped why anyone would do that.
CE Mark For Blockade Medical™ Barricade Coil System™
Another in a long line of Californian medtech start-ups, Blockade Medical™ has announced the gaining of CE Mark status for its Barricade Coil System™, designed to remove or endovascularly occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels.
CE Mark For autoRIC™ Remote Ischemic Conditioning Device
Canadian company CellAegis Devices, Inc., has announced that it has received a CE Mark for its autoRIC™ Device, which the company says for the first time allows simple, consistent, reliable and cost-effective automation of remote ischemic conditioning at the point of care.
Now Xlumena’s Axios Stent CE Mark Approval Includes Biliary Tract Drainage
Xlumena, Inc. has announced that it has received CE Mark approval to market its AXIOS Stent and Delivery System for biliary tract drainage. The device was previously approved for the treatment of pancreatic pseudocysts.
CE Mark For MEDIHONEY® HCS Coincides With BMJ Paper Supporting Honey Application In Acute Wounds
In one of life’s pleasing little coincidences a newly published meta-review of wound care studies has, among its conclusions, established that topical honey reduces wound healing time when compared to film or gauze-based dressings for burns. Derma Sciences, Inc., with perfect timing has announced the CE Marking for its patented MEDIHONEY® HCS (hydrogel colloidal sheet) dressings, containing (you’ve guessed it), honey.
CE Mark For TranS1 VEO™ Minimally Invasive Lateral Access Fusion System
Minimally invasive lumbar spine device company TranS1 Inc., has announced it has received CE mark approval in the European Union to market its VEO™ lateral access fusion system for interbody fusions.