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In the UK, for example, the Medicines and Healthcare products Regulatory Agency (MHRA) acts as a CA. In Italy it is the Ministero Salute (Ministry of Health) Medical units must not be mistaken with medicinal products Within the EU, all medical devices should be identified with the CE mark The conformity of a medium or excessive danger medical system with relevant regulations can also be assessed by an exterior entity, the Notified Physique , before it may be placed on the market.