Elite Biomedical Solutions

Thoroughly cleaning infusion pumps is essential for patient safety. Follow these best practices for a comprehensive cleaning strategy: https://bit.ly/38inJsx

The FDA's final guidance for medical device remanufacturing is designed to ensure patients have access to safe, effective medical devices. Get more details on the guidance: https://bit.ly/3WkoaHF

Studies show that more than 75% of infusion pumps have some kind of cybersecurity vulnerability. Use our checklist to stay on top of security for these connected devices: https://bit.ly/3VUhXDo

Between supply chain challenges and medical device price increases, it's more important than ever to keep medical equipment running optimally for as long as possible. Get insight into how to do that: https://bit.ly/3I61eWK

Professional development for BMETs is often considered a non-essential expense, but here are 5 convincing reasons it shouldn't be: https://bit.ly/3ZJEXEb

Staying on top of infusion pump repairs and using quality replacement parts can transform the safety, efficiency, and longevity of the devices. https://bit.ly/3Jc8WhH

U.S. medical equipment manufacturers are urging lawmakers to implement tax incentives, enforce stricter labor and environment standards, and impose higher tariffs on foreign medical supplies to bolster domestic production. Read more via Becker's Hospital Review:

US devicemakers call for tax incentives, tariffs to bolster production: 4 things to know An alliance of U.S. medical equipment manufacturers is urging lawmakers to implement tax incentives, enforce stricter labor and environment standards and impose higher tariffs on foreign medical supplies to bolster domestic production, according to an Nov. 5 news release from the American Medical Ma...

When looking for medical device replacement parts, should you source them from an OEM or third party? Get insights in our guide: https://bit.ly/4aSislQ

The FDA designated 166 products under its breakthrough devices program in the 2024 financial year, reversing the downward trend following the COVID-19 pandemic. https://bit.ly/4fb11Pl

FDA breakthrough device decisions rebound after recent declines The FDA designated 166 products under its breakthrough devices program in its most recent financial year, reversing the downward trend seen as the COVID-19 pandemic eased.

Nearly 5 years after BD voluntarily recalled the Alaris infusion pumps, issues continue. Here’s an updated overview of the situation and tips for how to move forward. https://bit.ly/4iqlgLL

When it comes to infusion pumps, the adage "If it isn't broken, don't fix it" doesn't apply. Here's why: https://bit.ly/3YXkCO2

How can robots enhance plastics manufacturing? We explore the impact of using robotics in biomedical equipment manufacturing: https://bit.ly/3RilZC8