News | October 30, 2006

In an effort to address triple-digit increases in errors related to device use, the Biomedical Research & Education Foundation (BREF) has announced that it has formed a National Committee to develop a National Medical Device Registry. Founding partners are the University of Pennsylvania School of Medicine and the Cleveland Clinic Foundation.
The first phase of development will focus on monitoring and tracking the use of orthopedic devices. In the past decade, the number of medical technology patents and knee and hip replacements approximately doubled. Reports of adverse events related to medical products increased from 75,000 to 250,000 per year in the 1990s.
A device registry could allow for longer-term monitoring, facilitate more successful recall programs, increase reporting of adverse events and allow for quality and cost comparisons. In addition, it could provide medical professionals with critical information regarding device use, sterilization needs, compatibility with other devices and procedures, and allergy risks.


Additional Content

Sponsored Content | Whitepapers | Information Technology

The Interoperability Decision Every Imaging Operation Is Facing Integration protocol has become an operational and ...

Time October 25, 2026
arrow
News | Radiation Oncology

July 16, 2026 — Raidium has announced the U.S. launch of Raidium Read (R.Read), applying its AI-native imaging solution ...

Time July 16, 2026
arrow
Feature | PACS | John Freeland

People in healthcare technology love to talk about digital transformation like it just started happening. Cloud ...

Time June 29, 2026
arrow
News | Information Technology

June 26, 2026 — Radin Health recently announced the successful deployment of its cloud-native platform at four ...

Time June 26, 2026
arrow
News | Information Technology

June 24, 2026 — HOPPR Presto Agent (Presto) is now commercially available from HOPPR. Presto iis a tool that ntegrates ...

Time June 24, 2026
arrow
Subscribe Now