Case Study: Teleflex Incorporated achieves UDI compliance and a single trusted product-data source with LANSA

Harnesses Strong Partnerships to Build a Sustainable Pim System for Regulatory Compliance, Patient Safety, and Customer Engagement

Teleflex, a global maker of specialty medical devices, needed to comply with the U.S. FDA’s Unique Device Identification (UDI) rule while preparing for future global regulations and customers’ expectations for trusted product data. The company’s challenge was consolidating diverse legacy systems and processes to reliably assign, validate and share device identifiers and attributes.

Teleflex partnered with GS1 Solution Partners 1WorldSync and LANSA to deploy a GS1 Standards–based PIM and integration solution that centralized GTIN assignment, automated validation, and published verified records to the FDA’s GUDID and the GDSN. The outcome is a single source of truth for accurate, validated product data, improved supply-chain efficiency and regulatory compliance, and strengthened patient safety.

Teleflex Incorporated

Mark Hoyle

Technical Director, UDI