The FDA UDI Regulation establishes a single device identification system that is consistent, unambiguous, standardized, and globally harmonized. All manufacturers of medical devices will be required to comply with the new UDI methodology. The annual UDI Conference is the ONLY event dedicated to guidance and training for those impacted by the UDI Regulation.
The UDI Conference 2015 is specifically structured for implantable, life-supporting, and life-sustaining devices and Class II medical devices facing imminent compliance dates, as well as hospitals moving towards incorporating UDI data into existing systems.
In order to comply to the compliance regulations, all barcodes must receive a “C” grade. The only way to properly grade barcodes is with a barcode verifier. Verification will not only grade your codes, but will also provide you with the tools you need to identify errors in your printing process and how to correct them. Verification analyzes all of the parameters within a code, the format of the data within the code and if it meets industry standards.
Attending this year’s UDI Conference will give you a chance to learn everything you need to know to ensure your barcodes are compliant with FDA regulations. In addition, you can speak one on one with barcode experts. Stop by the Teklynk, PIPS, Webscan booth and we’ll provide you with a free assessment of your barcoding needs.
UDI Conference 2015
June 24th and 25th