What is a GS1? Shedding light on the UDI provider

Sören Hornof
Updated June 13, 2024
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Question

What is GS1? And how do we get GS1 UDIs?

Short Answer

GS1 provides “one global system” for product identification. It’s a company that sells numbers to businesses. Those numbers help identify the products throughout the entire supply chain. Medical device manufacturers use the GS1 system to create their UDIs.

Long Answer

GS1 is a global non-profit organization that develops and maintains standards for various industries to enable efficient business processes and seamless communication between trading partners. In normal words: it sells numbers to you and makes sure they are unique. GS1 operates 116 local subsidiaries and serves over 2 million user companies. Its headquarter is in Brussels.

By the way, we’ve recorded a step-by-step walkthrough video of how to get a MDR UDI from GS1, so take a look:

We also have an MDR UDI overview article which might be interesting for you, too.

The unique identification numbers, such as barcodes and product numbers help in identifying products, services, assets, and locations in supply chains and other business operations. GS1 standards are used in a wide range of industries, including retail, healthcare, food and beverage, logistics, and more.

Almost every barcode that you come across has been issued by GS1. Product codes come in the form of an EAN (European Article Number), a standardized barcode symbology used to uniquely identify products for retail and distribution purposes. EANs are a subset of the broader GTIN (Global Trade Item Number) system developed by GS1. The primary function of an EAN is to provide a scannable code that represents product information and allows for quick and accurate data entry in retail and supply chain systems.

In the context of healthcare, GS1 standards play a crucial role in ensuring patient safety and regulatory compliance. In the European Union, the Medical Device Regulation (MDR) requires medical device manufacturers to assign Unique Device Identifiers (UDIs) to their products. GS1 standards are the most common way to achieve this. It’s not the only option though.

On a slighty different note: You want to get your medical software certified under MDR but don’t know where to start? No worries! That’s why we built the Wizard. It’s a self-guided video course which helps you create your documentation yourself. No prior knowledge required. You should check it out.

Or, if you’re looking for the most awesome (in our opinion) eQMS software to manage your documentation, look no further. We’ve built Formwork, and it even has a free version!

If you’re looking for human help, did you know that we also provide consulting? We’re a small company, so we can’t take on everyone – but maybe we have time for your project? We guide startups from start to finish in their medical device compliance.

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