MDR certification (IMC Consultant)
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  • MDR certification (IMC Consultant)

MDR certification (IMC Consultant)

MDR certification (IMC Consultant)

A medical device is intended to detect, alleviate or prevent ailments, diseases or handicaps in humans. This includes a wide variety of products, ranging from plasters, wheelchairs and other aids to the most complex life support equipment. Medical devices must now comply with the European Directive 93/42 / EEC (MDD), with effect from May 2020, the European Regulation 2017/745 / EU (MDR) must be definitively met. Medicines and aids intended exclusively for clinical research are not covered by this guideline.

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