Assistant for product classification according to EU MDR 2017/745.
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Use This GPTSuggests the correct MDR classification for your medical device based on the MDR Annex VIII Classification Rules. Please provide a description of your...
💬 10+ Chats
Expert in EU medical device registration, offering downlink to download regulation documents and guidance on MDR
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Conversational guide to EU MDR, IVDR, and MDCG guidance documents, with clear, bullet-pointed answers.
💬 4+ Chats
Guides on AI healthcare device compliance with EU MDR, using uploaded documents.
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Find the 10-digit Harmonized System (HS) code required for products imported into Canada.
💬 10+ Chats
Provide an Article and use our powerful Sentiment Classifier
💬 40+ Chats