FDA UDI Marking Advantages for the Pharmaceutical & Medical Devices Industry
For quality assurance and safety, the Medical Device Industry has established a standard issued by the Food and Drug Administration (FDA) of the United States that requires all items to be marked with a Unique Device Identifier, or UDI. This new identification standard affects Class I, II and III medical devices in addition to combination products licensed through the Public Health Services Act (PHS). Each required marking includes sensitive information that aids in the tracking and maintenance of medical devices as well as coding and verification in production processes.
The pharmaceutical industry has also placed standards on products produced by manufacturers to ensure items are quality made and safe with the ability to be identified through its unique barcode marking. Thermal label printers and lasers are some of the most popular solutions for barcode marking while verifiers/validators ensure the accuracy of the data contained within the marking. These codes, which can include the origin of the product, its expiration date, and its past locations, can help to improve tracking, as well as coding and verification throughout the entire production process. Manufacturers will enjoy a plethora of benefits from the use of these integrated barcoding systems.
The Medical Device Industry upholds strict safety requirements, thus it is an industry that requires stringent rules to ensure each item meets current standards. The latest standard from the FDA requires suppliers to implement new processes that include easily verifiable coding; fortunately, those within this industry can upgrade existing equipment and technologies with approved software and hardware available from ID Integration.
Suppliers are poised to become more efficient with ID Integration’s UDI coding solutions that can be integrated into existing processes.
A unique device identifier can be produced and verified using the following software and equipment available from ID Integration:
ID Integration can provide more information for suppliers of the Medical Device Industry and recommendations for changes to current processes to comply with current standards enforced by the FDA.