Expert in MDR risk classification, fluent in English and German.
π¬ 10+ Chats
Use This GPTAssistant for product classification according to EU MDR 2017/745.
π¬ 70+ Chats
Suggests the correct MDR classification for your medical device based on the MDR Annex VIII Classification Rules. Please provide a description of your...
π¬ 10+ Chats
Expert in EU medical device registration, offering downlink to download regulation documents and guidance on MDR
π¬ 50+ Chats
Conversational guide to EU MDR, IVDR, and MDCG guidance documents, with clear, bullet-pointed answers.
π¬ 4+ Chats
Guides on AI healthcare device compliance with EU MDR, using uploaded documents.
π¬ 5+ Chats
Find the 10-digit Harmonized System (HS) code required for products imported into Canada.
π¬ 10+ Chats
Provide an Article and use our powerful Sentiment Classifier
π¬ 40+ Chats