Udi Medical Device Labeling

A class i device with a universal product code upc on the label and packages meets the udi requirements.

Udi medical device labeling.

To be specific the concept of udi did appear on the imdrf guidance issued in 2013 this defined the basis of this new technology. The unique device identification system final rule udi rule requires device labelers typically the manufacturer to. Dates on the labels of devices excepted from or not subject to the udi labeling requirements must be formatted as required by 801 18. This element will be key for the traceability of devices in europe.

This means the upc is the di. Using an automated udi labeling system can keep your medical device manufacturing business running smoothly. The udi or unique identification number europe as there is also one in the usa is one of the new things that come with the new eu mdr 2017 745 and ivdr 2017 746. Mft 350 or mft 550 ip3.

Food and drug administration fda created unique device identification often abbreviated udi a rule that requires medical device manufacturers to label their products and in some cases direct product markings with both a unique device identifier and production identifiers such as expiration date and lot or serial number. Udi registration for devices. Some class i devices are of such low risk that fda exempts them from the 21 cfr 820 except. Unique device identification udi labeling systems best recommended with.

Implementing udi labeling for medical devices though it s been a few years since the the fda s unique device identification udi rules came into effect there remains quite a lot of confusion among medical device manufacturers about exactly how to label products. Medical device regulation mdr regulation eu 2017 745 of the european parliament and of the. Class i and unclassified medical devices compliance date. The udi of a class i device is not required to include pis.

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 readable interpretation based upon. Registration of manufacturers and economic operators. The manufacturer must provide all the gudid information. When fully implemented the label of most devices will include a unique device identifier udi in human and machine readable form which will ultimately improve patient safety modernize device.