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Medical Device Machinists Are Multi-Task Masters Medtech machining equipment has evolved to meet customers’ demands for micro components, material variability, more complex shapes, and tighter.

Navigating Current Challenges with Sterilization Capacity Constraints In recent years, the medical device industry has faced growing sterilization capacity constraints. The primary causes are.

Sopheak Srun Appointed Co-Chair of an AAMI Working Group Sopheak, QTS Principal Sterilization Specialist, will be contributing to new and existing ISO standards to be upheld internationally.

Compliance to the UDI regulation includes the FDA public database, GUDID. The first phase of the Global Unique Device Identification Database (GUDID): Guidance for Industry document is now available..

DuPont Tyvek Transition Update DuPont is transitioning Tyvek® 1073B and Tyvek® 1059B to manufacturing lines that use the latest flash-spinning technology to help ensure greater continuity and.

Unique Device Identification (UDI) Final Rule was announced by the FDA on September 20, 2013. The rule was published in the Code of Federal Regulations as of September 24, 2013. Implementation for.