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Hamburg - Local Division UPC_CFI_553/2025 Final Order of the Court of First Instance of the Unified Patent Court delivered on 21/10/2025 HEADNOTES: 1. Since a CE marking is required for placing a medical device in any of the EU member states, obtaining such a CE-mark approval gives an indication of an expected market entry of the device in any of the EU member states including in Germany in the foreseeable future (Art. 5.1 regulation (EU) 2017/745 on medical devices, Art. 33 (1) lit. a UPCA). 2. By obtaining (and publicly announcing) CE -mark approval for the attacked (implantable) medical devices , providing “ordering information” and announcing to show -case their products on a trade fair, the Defendants have set the stage to market these products , R. 206.2 lit. c) RoP. 3. As CE-mark ap ...