European Real-World Registry for Use of the Ion Endoluminal System

Prior treatment

• Patient is participating in an interventional research study or research study with investigational agents with an unknown safety profile that would interfere with participation in this study or study results.

Other

• Female patient that is pregnant or breast feeding as determined by standard site practices.
• Patient is legally incapacitated or in a legal/court ordered institution or is part of a known vulnerable population, including but not limited to dependency on the sponsor, hospital or study doctor.
• Patient is not willing to comply with post-procedure study participation requirements.
• Investigator, in their professional opinion, has decided that it is in the patient's best interest to not participate in the clinical study.

• Patient is aged 18 years or older at time of consent.
• Patient is planned to undergo a lung lesion biopsy(s) and/or localization procedure(s) utilizing the Ion endoluminal system.
• Patient is willing and able to give written informed consent for clinical study participation.