How do EU export controls impact a French manufacturer exporting medical devices to non-EU markets?

Hello, I came across your question regarding EU export controls for French medical device manufacturers. Navigating these regulations can be quite complex, as it involves understanding the EU Dual-Use Regulation (2021/821), specific product classifications, and licensing requirements for non-EU markets. Ensuring full compliance is crucial to avoid penalties. I can provide a low-cost consultation via WhatsApp to walk you through the applicable controls, classifications, and typical timelines for your specific products.