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

Question

We are a French manufacturer of medical devices looking to export to partners outside the EU. What licenses or classifications apply under EU export controls, and what is the typical timeline? We want to avoid penalties and ensure full compliance.

mohammad mehdi ghanbari · Accepted Answer

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.

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

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