Novation Supports FDA’s Proposed Unique Device Identification Rule

Novation has called the FDA’s proposed rule implementing a Unique Device Identification system for medical devices a “significant milestone for patient safety,”according to a news release.

Advertisement

 

“A robust UDI system will significantly enhance product identification, improve the device recall process, and ensure the integrity of the product throughout the transportation process, and most importantly, advance and improve patient safety,” said Dan Sweeney, senior vice president of information and data services at Novation, in the release. “A UDI system also has the potential to generate significant savings for the health care industry through improved efficiencies and automated processes. Given the dramatic changes in finances and urgent patient safety needs, health care organizations and patients will benefit most from a swift implementation of a UDI system.”

 

Novation, a supply contracting company for the members and affiliates of VHA, UHC, Children’s Hospital Association and Provista, said it has been an advocate of UDI implementation for several years.

 

FDA issued the proposal on July 3.

 

Related Articles on Medical Devices:

Intrinsic Medical Imaging Receives FDA Clearance for 3D Imaging Workstation

Teleflex Receives FDA Clearance for Peripherally Inserted Central Catheter

Abbott Receives FDA Clearance for Cataract Surgery Protective Gel

Advertisement

Next Up in Uncategorized

Advertisement

Comments are closed.