The Risks of Last-Minute Device Registration – And How to Avoid Them

With increasing global UDI regulatory demands like EUDAMED in the EU, GUDID in the US, and now AusUDID in Australia, medical device manufacturers are under pressure to ensure timely and accurate registration of their products. While some companies manage to stay well ahead of compliance deadlines, others find themselves scrambling to submit device data at the last moment.

Registering medical devices to a regulatory database close to the mandatory deadline may seem harmless, but it can introduce significant risks to your business. Below, we outline the potential challenges and offer strategies to help you proactively manage and reduce these risks.

 The Hidden Risks of Late Registration

1. Potential System Overload
   Regulatory systems like EUDAMED are complex and handle massive volumes of data from thousands of manufacturers. For example, an expected 5-6 million records will be submitted to EUDAMED by over 30,000 medical device manufacturers across the European Union. Submitting close to the deadline increases the chance of encountering slow response times, timeouts, or full system outages. These delays could prevent successful registration within the required timeframe.
2. Higher Error Rates
   When teams rush to meet deadlines, quality often suffers. Data errors — from incorrect formats to missing fields — are more common during last-minute submissions. These mistakes can lead to rejections or require resubmission, further compounding time pressure.
3. Limited Time for Issue Resolution
   If your device submissions are rejected or flagged for errors, there may not be enough time left to fix the problem and resubmit. This puts your compliance, and consequently your ability to sell your products, at serious risk.
4. Regulatory and Business Impact
   Failure to meet UDI registration deadlines can result in regulatory sanctions, such as product delisting, fines, or loss of market access. It can also damage your reputation with regulatory bodies and affect customer confidence.
5. Strain on Internal Resources
   The end-of-cycle rush puts immense pressure on regulatory, quality, and IT teams. This stress can lead to burnout, rushed decision-making, and long-term operational inefficiencies.

 How to Mitigate the Risks

1. Start Early and Plan Ahead
   Begin UDI data preparation well in advance of regulatory deadlines. Early starters can voluntarily submit their devices, validate data more thoroughly, and troubleshoot without pressure.
2. Implement a Reliable Global UDI Solution
   Use a centralized UDI data management platform with robust data validation, workflow and RBAC (role-based access control) to streamline collaboration, approvals, and submissions across global teams.
3. Validate and Simulate Submissions
   Use tools that let you validate device data against the specific business rules of each regulatory database (like EUDAMED or GUDID) before submission. Simulation testing in pre-production environments provided by the regulatory bodies helps catch errors early and gives you enough runway to take corrective action.
4. Maintain Strong Documentation and Governance
   Govern your UDI data with clear data ownership, documentation, and change control to reduce last-minute confusion, streamline collaboration and ensure audit readiness.
5. Work with Trusted Partners
   Engage UDI solution providers with a global presence and have a proven track record of successful UDI implementations. UDI is increasingly a global initiative, and scalability is paramount – trusted partners can help you navigate complex requirements and avoid costly missteps.

Final Thoughts

In the race to meet global UDI compliance, timing is everything. Late submissions increase risk, reduce flexibility, and can directly impact your ability to sell and support medical devices in critical markets.

The good news? These risks are entirely avoidable. With the right strategy, tools, and partners, manufacturers can simplify compliance, avoid the last-minute scramble, and build a foundation for long-term regulatory success.

At Innovit, we are proud to have delivered proven UDI compliance solutions that enable leading medical device manufacturers to achieve global UDI compliance— faster, easier, and with confidence.

Note: UDI (Unique Device Identification) efforts are global in nature with countries and regions introducing their own systems for uniquely identifying medical devices to ensure traceability and patient safety.