EU Medical Devices Regulation (EU MDR) Data Services

Compliance with EU MDR Becomes Mandatory in May 2021

In May 2017, the EU Commission published the Medical Devices Regulation (MDR). The regulation becomes mandatory for medical device producers as of May 26, 2021.

(The original mandatory application date for the EU MDR was May 26, 2020, but the date was postponed by one year, until May 2021, due to the COVID-19 pandemic.)

The EU MDR replaces the previous Medical Device Directive (EU MDD) and Active Implantable Medical Device Directive.

EU MDR changes how medical devices are defined, how devices are classified for risk, and creates a new labeling system. The regulation also includes certain substance content requirements.

Under the new EU MDR, medical devices cannot contain substances classified as carcinogenic, mutagenic, or toxic for reproduction (CMR 1A/1B) or endocrine-disrupting substances (EDS) in amounts over 0.1% w/w without justification. The use of latex, as well as substances of human or animal origin, must also be declared if present.

Get Help With Substance Data

As part of our Data Services, we will collect substance data from your suppliers on your behalf, and check it against the lists of applicable CMR 1A/1B and endocrine-disrupting substances addressed under the EU MDR, using our powerful, purpose-built GreenData Manager compliance software.

We leverage the Full Material Declaration (FMD) data already in our component database to cut down on collection time. And we can help with EU RoHSEU REACH SVHC, and other global regulations.

Plus, we will track the regulations you are complying with for updates and new substance additions and alert you when there are changes to ensure you are always showing up-to-date compliance.

We can even collect information on the presence of animal and human derived materials, as well as latex, as required by the EU MDR.

GreenSoft Technology: A Trusted Partner

medical devices testimonialAt GreenSoft, we have over 15 years of experience in managing compliance data.

We currently work with many medical device manufacturers of all sizes.

We have a broad range of expertise in active and passive components, electrical and mechanical parts, packing and printing materials, and raw materials including organic or non-organic chemicals. GreenSoft has relationships with over 32,000 suppliers worldwide and is ISO 9001:2015 certified.

Contact Us Today to Learn More and Get Started

Our EU MDR Data Services provide you with the substance data you need to enable your product to be submitted to the UDI database, and evaluated by a notified body for approval, while freeing up your time to focus on other elements of the product approval process.

Contact us to learn more or request a demo. We will provide you with a FREE Risk Analysis/BOM Scrub when you contact us today.

Bonus: view a recording of our EU MDR webinar!

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