Everything You Need to Know About EU Regulation 2025/1234 and the Future of eIFU for Medical Devices

On July 16, 2025, a pivotal regulatory update—EU 2025/1234—comes into effect, expanding the use of electronic Instructions for Use (eIFU) to a much broader range of medical devices and accessories. Unlike previous regulations that limited eIFU to implantables or certain fixed devices, this amendment now authorizes the use of eIFU for all professional-use medical devices, including those covered by transitional provisions and even non-medical products listed under Annex XVI.

This shift marks a turning point in the digitization of compliance documentation in the medical device industry. In this video, we walk you through the full impact of the new regulation, as well as the operational benefits and responsibilities that come with adopting eIFU.

🔎 What the regulation says:

Manufacturers are allowed to provide eIFUs for professional-use devices, as long as the device is not likely to be used by laypersons.

For any device that might be used at home or by a non-professional, a paper IFU is still mandatory.

All versions of an eIFU—current and obsolete—must be hosted securely and remain accessible to authorities on request.

The URL of the eIFU must be registered in EUDAMED's UDI database once that requirement becomes mandatory.

📌 Top 5 reasons why switching to eIFU makes sense:

Broader regulatory permission

Significant cost savings and faster updates

Improved traceability and audit readiness

Better experience for healthcare professionals

Alignment with the EU’s digital vision

🛑 But eIFU is not a one-size-fits-all solution. You still need paper IFUs in key scenarios:

If your device could be used by laypersons, you must provide a paper version.

In low-connectivity settings, such as field hospitals or rural clinics, physical IFUs may be more reliable.

Adopting eIFU requires full platform readiness, including hosting, backups, multilingual versions, and internal QA validation.

Regulatory responsibility is now entirely on the manufacturer—including website uptime, version archives, and EUDAMED linkage.

Some stakeholders—including auditors and hospitals—still prefer traditional paper documentation, which could delay full adoption.

📽️ Watch our video to get a complete overview of the regulation and see how EasyIFU helps you implement a compliant, secure, and future-ready eIFU process. This is essential for RA/QA teams, product managers, and any manufacturer operating under MDR.