Webinar Series on Unique Device Identification

The Medical Device Regulatory Convergence Project co-lead by USAID, ANSI, and AdvaMed through the Inter-American Coalition for Regulatory Convergence in the Medical Technology Sector collaborated with the United States Food and Drug Administration (FDA) to organize a webinar series on Unique Device Identification.

Objective: Provide an overview of the requirements related to Unique Device Identification (UDI) and FDA’s perspective and experience implementing these requirements

Session I – 20 January 2022

Agenda

Recording

Presentations

Vision for Global UDI System:

Indira Konduri, FDA

Helio Filho, ANVISA

Overview of UDI and IMDRF documents

Session II – 27 January 2022

Agenda

Recording

Presentations

Industry Experience implementing UDIs: John Terwilliger, Abbott

Healthcare provider experience implementing UDIs: Cynthia Shumway – Intermountain Healthcare

Regulators Experiences:

ANVISA – Hélio Filho

ARCSA – Xavier Quintero

FDA – Indira Konduri

Minsal – Óscar Marín