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The AIM NA Public Policy Healthcare UDI Work Group responded to the International Medical Device Regulators Forum's (IMDRF) call for consultation regarding their proposed UDI guidance documents. The group’s comments focused on the effective use of AIDC technologies in meeting the FDA’s requirements for direct marking of devices for unique device identification purposes. To view the team’s comments, download the AIM NA IMDRF Public Consultation submission.
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January 2020
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