Independent Device Evaluation

Q: How can manufacturers use the results?

Permitted use : Suppliers can inform customers that their product has been evaluated and that the content is posted on the ECRI website. Suppliers may mention the title and date of the posting, and provide a link (note: access is available only to members of certain ECRI programs). Prohibited use : Suppliers or their representatives may not selectively quote from Device Evaluation content when communicating with customers. Suppliers also may not make any statements that imply that ECRI endorses their product or that a special or preferential arrangement exists. Suppliers may not quote from, paraphrase, or reproduce ECRI's findings, logos, taglines, or banners in advertisements or in promotional or marketing literature, without prior written approval of ECRI.

In-depth insights from the only independent device testing lab in the nation.

Empower your organization with independent insights.

When it comes to making smart buying decisions, you need objective, evidence-based research and recommendations. As the nation's only independent medical device testing organization, ECRI conducts hands-on rigorous testing and evaluation of devices that informs real-world technology decision making across all care settings. No other private sector organization in North America assumes this responsibility or provides this level of information and assurance.

Objective Results You Can Trust

Leveraging independent laboratory testing, specification recommendations, and direct user experience we identify products that outperform and are safer than those with significantly higher prices. From exploring and purchasing to operating and maintaining medical technology, ECRI provides a solution that empowers you with the independent insights you need to make the best and most well-informed decisions.

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Views generated by our Problem Reporting Network

Categories of devices evaluated

Why We're Unique

Our team of engineers and scientists are passionate about safety. If a hazard is identified while evaluating a device, it is immediately vetted and published to reduce preventable harm. Our evaluations focus on devices that not only cover the continuum of care but also the spectrum of technology including cutting-edge, AI-driven innovation.

Each evaluation is conducted using a test methodology developed by clinical reviewers, manufacturers, and internal experts.
All participating vendors can comment on testing methodology, and the methodology is applied equally to all evaluated devices to produce a fair comparison.

Results are presented using our five-star rating scale, and are obtained through hands-on testing by engineering staff at our laboratory, as well as through review of available clinical evidence.
All results are reviewed externally by clinicians and participating manufacturers before publication.

The Industry's Strictest Conflict-of-Interest Policy

For more than five decades, our strict conflict-of-interest (COI) policy has provided assurance about the integrity of our work. Our COI policy applies to our entire staff, extending beyond financial interest to include emotional and intellectual conflicts or bias.

INDEPENDENT DEVICE EVALUATION

FAST FACTS

Do you certify medical products?

No. We do not test to IEC or ISO standards (such as ISO 13485), and we do not offer any certification or product labels as a result of our testing.

Who can see the published results?

Evaluations are accessible by clients who are members of ECRI's Device Evaluation, Device Evaluation Plus, and Capital Guide programs.

Does ECRI charge manufacturers to participate?

No. We do ask manufacturers to loan or provide access to equipment and accessories free of charge.

How can manufacturers use the results?

Permitted use: Suppliers can inform customers that their product has been evaluated and that the content is posted on the ECRI website. Suppliers may mention the title and date of the posting, and provide a link (note: access is available only to members of certain ECRI programs).

Prohibited use: Suppliers or their representatives may not selectively quote from Device Evaluation content when communicating with customers. Suppliers also may not make any statements that imply that ECRI endorses their product or that a special or preferential arrangement exists.

Suppliers may not quote from, paraphrase, or reproduce ECRI's findings, logos, taglines, or banners in advertisements or in promotional or marketing literature, without prior written approval of ECRI.