3 Important Trends for Medical Device OEMs in 2024

By on February 13th, 2024

The medical device industry never stands still as patient and clinician expectations evolve, new technologies are developed, and regulations change. As a result, continuous improvement and adapting to change are

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Top 5 Uses for PICC Lines and Midlines

By on October 5th, 2023

PICC (peripherally inserted central catheters) lines and midlines are both highly effective and versatile vascular access devices. Both are used for treatments that require medications to be given repeatedly over

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Vascular Access for Hemodialysis – Choosing the Right Components for Your Device

By on August 31st, 2023

Hemodialysis is the most common method of treating kidney failure and end-stage kidney disease. It is a complex therapy that requires coordination between multiple healthcare professionals as well as, often,

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Galt Medical Launches New Vascular and Interventional Medical Devices Product Catalog

By on August 10th, 2023

This summer saw the launch of our Vascular and Interventional Medical Devices Product Catalog. It is a comprehensive resource for OEM customers, medical device buyers, and healthcare professionals as it

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Future Trends in Interventional Radiology

By on June 21st, 2023

Interventional radiology (IR) is a field of healthcare that constantly moves forward as innovative new technologies are introduced and the capabilities of clinicians become more widespread and advanced. Percutaneous electrochemotherapy,

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The Advantages of Using Micro Access Devices Versus Standard Access

By on May 3rd, 2023

Micro access devices are commonly used for a range of interventional radiology procedures, and they have been for some time. There is also a growing trend in other specialties to

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Selling Products Under Your CE Mark or Your Supplier’s – Top 5 Considerations

By on March 1st, 2023

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

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What the EU MDR Extension Means for Medical Device Buyers

By on January 31st, 2023

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,

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7 Trends in the Medical Device Industry for 2023

By on December 16th, 2022

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

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The Impact of MDR on Medical Device Availability in the EU

By on November 30th, 2022

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

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