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Medical Devices
14
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12/6/2022

Non-compliant medical devices: what are the risks?

Knowing the risks related to the non-compliance of your medical devices allows you to build an efficient business model. In order to reduce the time to market of your devices and the risks related to non-compliance, you can already adapt to the new regulation. Discover here the stakes of compliance.
Medical Devices
7
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12/6/2022

Regulation 2017/745 on DM: what are the major changes?

Regulation 2017/745 on medical devices will come into force on May 26, 2021. After seeing its first deadline pushed back by one year due to the Covid-19 pandemic, it will come from this date to impose new obligations on the various economic operators of the medical device industry. Here is a quick summary of the key points to remember.
Medical Devices
27
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12/6/2022

5 questions about... the new European regulation on medical devices

Although its implementation has been delayed for a year, the new medical device regulation means a lot of changes for companies. It's important to prepare now. EcoMundo reveals the answers to the 5 most common questions on the subject.
Medical Devices
4
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12/6/2022

Medical devices: will you have to re-certify them?

With the new European regulation on medical devices coming into force in May 2020, manufacturers need to be well prepared for the upcoming regulatory changes. What about medical devices already on the market under the old directives?
Medical Devices
29
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12/6/2022

Medical devices: the new European regulation, applicable in 2020

With the entry into force of the new regulation on medical devices in the European Union, more products are now covered. Non-medical devices are now included in the scope of the regulation.
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Authors

Christian Freneuil
Fang Zhou
Jeanne Pontisso

ECOMUNDO

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