2016 UDI deadlines are fast approaching. Are you ready?
Learn more about the requirements of UDI. Download our UDI infographic.
The FDA is phasing in unique device identification (UDI) requirements to identify medical devices throughout product lifecycle.
Effective from September 2016:
- Permanent UDI marking must be present on reusable Class III devices
- UDI marking must be present on labels and packaging of Class II devices
Videojet can help you understand the production implications of the 2016 deadline and identify the ideal coding solution for your products.