FDA updates UDI policy for direct marking of medical devices

By Stewart Eisenhart, Emergo Group

The US Food and Drug Administration has revised its Unique Device Identification (UDI) regulation’s direct mark requirements and compliance deadlines in response to cost and inventory concerns raised by industry.

Get the full story here at the Emergo Group’s blog.

The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.

The post FDA updates UDI policy for direct marking of medical devices appeared first on MassDevice.

from MassDevice https://ift.tt/2AxWMMH