Unique Device Identifier Udi

The first is the udi which is a unique number assigned to the version or model of a device that is required on all packaging labeling of finished goods.

Unique device identifier udi.

The udi consists of two parts. It was signed into law in the us on september 27 2007 as part of the food and drug administration amendments act of 2007 the eu acted to adopt udi and on april 5 2017 under the eu medical device regulation mdr and in vitro diagnostic regulation. Unique device identifier udi global enterprise labeling system gels inventory control forms 29 inventory control form. Include a unique device identifier udi on device labels and packages.

A udi is a numeric or alphanumeric code that is assigned to a medical device. This element will be key for the traceability of devices in europe. The unique device identification system final rule udi rule requires device labelers typically the manufacturer to. The unique device identification udi system is intended to assign a unique identifier to medical devices within the united states and europe.

A unique device identification udi system is intended to provide single globally harmonized positive identification of medical devices through distribution and use requiring the label of devices to bear a globally unique device identifier to be conveyed by using automatic identification and data capture and if applicable its human. Di device identifier a fixed section of the udi that identifies the specific model of device and the labeler. The udi must include a device identifier di and may contain a production identifier pi. Include a unique device identifier udi issued under an fda accredited issuing agency s udi system on device labels device packages and in some instances directly on the device.

The udi system consists of three core segments. To be specific the concept of udi did appear on the imdrf guidance issued in 2013 this defined the basis of this new technology.