Medical Device UDI & Regulatory Compliance Resources

Medical Device SolutionsResources library
Case studies

Reed Tech SingleSource™ for Drug Products and Schlafender Hase® TVT®, the Text Verification Tool®

Working together to help ensure that pharmaceutical companies and their products are compliant with global regulatory standards. Both companies understand and solve industry challenges with responsive solutions.

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How Kenmark Eyewear Created a UDI Strategy for Current and Future Challenges

How a global provider of world-class eyewear brands leverages Reed Tech SingleSource™ for Medical Devices

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How to Gain Regulatory UDI Submission Efficiencies with Reed Tech SingleSource™ for Medical Devices

How to Gain Regulatory UDI Submission Efficiencies with Reed Tech SingleSource™ for Medical Devices

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Recent blogs

What Global Manufacturers Need to Know About 2026 UDI Enforcement

US FDA Class I UDI Submission Deadline

Swissmedic Launches UDI Module in swissdamed

FDA Updates Guidance on GUDID and GMDN Codes: What You Need to Know

UDI Labeling (Unique Device Identification): Best Practices

UDI Regulations from EU, US, and other Global Regions

EUDAMED-Now or Later?

​​Expert Insights on the EU Proposed Legislation EUDAMED Rollout​-Approved

Understanding Basic UDI-DI in EUDAMED

​​Update on EUDAMED Timeline​
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Data sheets

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Product Data Availability for GS1 Compliance

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MedTech Compliance Solutions and Service

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Ultimate Guide to UDI For Medical Devices

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Reed Tech SingleSource™ for Medical Devices

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UDI Data Solutions for Medical Devices

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UDI for the C-Suite

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Medical Device Terminology

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South Korea – Intro to UDI

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China NMPA – Intro to UDI

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Reed Tech is now LexisNexis Life Sciences Solutions

While the Reed Tech name is being retired, the business has long operated as part of LexisNexis. Customers will continue to work with the same regulatory experts, services, and solutions—now unified within LexisNexis Life Sciences to reflect the broader capabilities and global resources of LexisNexis.