This clinical investigation will assess the self-adhesive properties of two investigational devices compared to a test specimen reference.
Participants who are capable and willing to comply with protocol visits, assessments, and instructions.
Participants must be in general good health with healthy and intact skin in the test area (as determined by the investigator based on medical history and examination of the application sites).
Minimal hairiness at the back (location of the application sites).
Signed written informed consent.
Known allergy/hypersensitivity to the dressing or its components.
Participants with any features at the application sites will be in contact with the adhesive surface of the dressing, and could influence the investigation.
Participants not willing to avoid contact of the application sites with water in the morning prior to dressing application and throughout the entire course of the study.
Participants not willing to avoid applying any detergents to the application sites in the morning prior to dressing application and throughout the entire course of the study.
Map coordinates are unavailable for these locations. Locations are shown below instead.
Germany