TactiFlex Duo builds on Abbott’s electrophysiology portfolio with a catheter than can ablate irregular heart rhythms using ...

Rockfield Medical Devices Limited Receives CE Mark Approval for the Mobility+® Enteral Feeding System, Marking a Major ...

Abbott’s latest CE mark for its TactiFlex Duo system was based on a clinical trial conducted in the European Union, United ...

Abbott supported its CE mark approval with data from its FOCALFLEX CE mark study. The global clinical trial, conducted across ...

CMR becomes the third surgical robotics company alongside Intuitive Surgical and SHURUI Robotics to obtain a CE mark in ...

CMR Surgical received the approval for abdominal surgery for its Versius platform in patients under age 18 in Europe, while ...

CMR Surgical announced today that it received CE mark and UK approval for its Versius surgical robot in pediatric surgery.

Only a month after Getinge announced the suspension of the CE marks allowing it to sell its heart-lung support and permanent life support systems in Europe, the Swedish devicemaker has temporarily ...

The UPC has granted a preliminary injunction effective for Germany, France, Italy, the Netherlands and Ireland against a Chinese medical device manufacturer and its Dutch subsidiary over the ...

Hyperfine today announced that its FDA-cleared portable magnetic resonance (MR) brain imaging system, called the Swoop system, has gained CE approval for its latest generation of AI-powered software.

Getinge is facing a huge roadblock with its life support systems in Europe. The Getinge, Sweden-based company said last week it received notification from DEKRA, the notified body for certification ...