MDR is the name given to the practices know as Medical Device Regulations as a whole. This practice, which entered into force on May 25, 2017, is an arrangement introduced within the scope of reassessment of medical devices although their compliance has been certified before.
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Machine CE Certification is the certification process carried out within the framework of the conditions introduced by the European Union. This certification aims at avoiding the negativities that might threaten the health of both humans and the environment during the production, assembly and use of machinery.
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