Regulation 2017/745 on medical devices, two major innovations: 1) the physiological action of devices consisting of natural materials such as vegetal matrices; 2) the chemical-physical-mechanical action of devices made of "substances", which as such are artificial derivatives
The Medical Device Regulation 2017/745 (MDR) enables the development of a wide range of innovative products. With respect to Directive 93/42, the MDR explicitly identifies the so-called "medical devices made of substances" (MDMS) through specific requirements. In addition, the MDR expands...
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Format: | Book |
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Frontiers Media S.A.,
2024-04-01T00:00:00Z.
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A1234.567 |
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Copy 1 | Available |