EPIONE Guided Lung Evaluation

Interventional clinical study to obtain performance and safety data of the EPIONE® device when used for percutaneous procedures in the lung.

Inclusion Criteria:Patient ≥18 years old,Patient for whom a percutaneous CT-guided intervention in lung has been prescribed and agreed by a multidisciplinary team of radiologists, surgeons and clinicians,Patient with a signed informed consent form.Patient covered by a social security system.Exclusion Criteria:Patient unable to undergo general anesthesia,Pregnant or nursing female, confirmed before the interventionPatient already participating in another clinical study