Expert in EU medical device registration, offering downlink to download regulation documents and guidance on MDR
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Assistant for product classification according to EU MDR 2017/745.
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Suggests the correct MDR classification for your medical device based on the MDR Annex VIII Classification Rules. Please provide a description of your...
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Conversational guide to EU MDR, IVDR, and MDCG guidance documents, with clear, bullet-pointed answers.
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Guides on AI healthcare device compliance with EU MDR, using uploaded documents.
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