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Manufacturers › Pharmaceutical Industry › Unique Device Identifiers

Hogan Lovells

FDA delays UDI database enforcement for low-risk devices

Hogan Lovells on

On July 25, 2022, the U.S. Food and Drug Administration (FDA) issued final guidance on Unique Device Identification (UDI) compliance date policies, stating that the agency will not enforce a requirement that manufacturers of...more

McDermott Will & Emery

FDA Extends Deadline for Removal of NDC and NHRIC Numbers from Device Labeling and Packaging

McDermott Will & Emery on

On August 30, 2016, the US Food and Drug Administration (FDA) published final guidance in which the agency announced it does not intend to enforce its prohibition against the inclusion of National Health Related Item Code...more

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