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Medical Devices

EUs MDR Date of Application Delayed Until 2021

In a major development for medical device manufacturers, the Parliament and Council of the European...

U.S. FDA Temporarily Eases Enforcement Policies for Certain Digital Health Devices

Moving quickly to address the need for advanced medical technologies during the COVID-19 outbreak...

FDA Updates Database of Recognized Consensus Standards for Medical Devices

The U.S. Food and Drug Administration (FDA) has updated its list of recognized standards...

EU Commission Extends MDR Transition Period for Certain Class 1 Devices

The EU has approved a “correction” to its Medical Devices Regulation (Regulation (EU) 2017/745,...

FDA Issues Draft Guidance on Safety of Medical Devices in MR Environments

The U.S. Food and Drug Administration (FDA) has issued a draft guidance on assessing...
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U.S. FDA Seeks Test Cases for Digital Health Software Precertification

As part of its effort to evaluate its precertification framework for software with medical...

FDA Issues Guidance on Medical X-Ray Devices and Conformity with IEC Standards

The U.S. Food and Drug Administration (FDA) has issued a guidance that addresses comparable...

FDA Issues Guidance on Premarket Submission Info on Performance Testing

The U.S. Food and Drug Administration (FDA) has issued a new guidance intended to...

U.S. FDA Issues Guidance on Medical Devices Containing Materials of Animal Origin

The Center for Devices and Radiological Health (CDRH) of the U.S. Food and Drug...

FDA Issues Guidance on Device Exemptions from Pre-Market Notification Requirements

The U.S. Food and Drug Administration (FDA) has issued a final guidance clarifying the...
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