Medtech Insight features interview with AMDR’s Dan Vukelich
Medtech Insight taps AMDR's Dan Vukelich as an industry expert for insight into how European member states are likely to respond to the EU's new Medical Device Regulation (MDR) which "introduces new and much tighter
Reprocessed Medical Devices Market To Grow to Over $3 Billion by 2024
A new report by Global Market Insights projects the global reprocessed medical devices market will surpass 3 billion USD by 2024. According to the report, the demand for reprocessed medical devices is fueled by increasing
Reprocessing: protecting assets and preventing medical device misuse
AMDR has been a long-standing member of the Association for the Advancement of Medical Instrumentation (AAMI), the premier standards setting organization for medical devices. Recent articles in AAMI publications, shed light on the issue of
AMDR Participates in Upcoming EU Conferences, Promotes Reprocessing and Remanufacturing of Single-Use Devices
AMDR continues its speaking and Conference tour of Europe to encourage Ministries of Health, healthcare professionals and other stakeholders to evaluate the provisions of the new European Medical Device Regulation (MDR) as Article 17 requires
Use of Catheter Reprocessing to Reduce Cath and EP Lab Costs: Aligning cardiology industry objectives with clinical and patient care goals
Diagnostic & Interventional Cardiology recently published the article, "Use of Catheter Reprocessing to Reduce Cath and EP Lab Costs", that explores the challenges and opportunities found within the EP lab setting. The article notes that
AMDR Members Unaffected by FDA Recall of Reprocessed Agilis Steerable Introducers from SterilMed
The U.S. Food and Drug Administration issued a recall of reprocessed Agilis Steerable Introducers from SterilMed, a unit of Johnson & Johnson, on product lots manufactured between January 1 and May 5, 2017. Agilis Introducer