Marking Guidelines, Methods, and Verification

The deadline for Class 2 Medical Devices governed by the FDA's Unique Device Identification (UDI) regulation took effect September 24, 2016 – and it's not just about your medical device packaging anymore! Join Omron Microscan for a presentation on the FDA UDI guidance for marking devices with permanent marks, marking methods, and verification solutions.

  • What does it mean to "permanently mark" a device?
  • What are the FDA's requirements for marking UDI codes?
  • What can be done to ensure mark quality and compliance?