All medical device products sold in the EU need a CE mark. For the lowest-risk medical devices, it is possible to use a self-certification CE marking process. However, for class
The EU medical device market is currently in a period of transition to a new set of regulations known as MDR – Medical Device Regulations. For a number of reasons,
Companies in the medical device industry continuously change and adapt through the development of new products and technologies. MedTech companies must also react to changing regulations, market conditions, and customer/patient
The EU MDR (Medical Device Regulation) is the new set of regulations for medical device products sold in the EU. The previous regulations, known as MDD (Medical Device Directive), will
Vascular access devices are used in hundreds of millions of procedures around the world every year. They have transformed patient outcomes through the development of innovative therapeutic and diagnostic procedures.
While transfemoral coronary interventions have a longer and more widespread history than transradial interventions, there is a growing body of evidence in favor of radial access. What is that evidence
PICCs (peripherally inserted central catheters) and implantable ports are both vascular access devices. Their primary purpose is to allow the repeated administration of drugs over a period of time. That
Tearaway introducers have been used over many years to enhance a wide range of minimally invasive medical procedures. Over this time, considerable advances have been made in the design of