Human Participant Study of Prototype Non-medicated Multilayer Foam Dressings on Intact Skin

Inclusion Criteria: * Participant is capable of providing informed consent * Participant is willing and able to make all required study visits * Aged 22-70 years at the time of signing the informed consent\* * Participant must be in good health, as determined by the Investigator, based on medical evaluation, including medical history and skin application site assessment (healthy intact skin at or near any of the dressing application sites) * Participant is willing not to use cosmetic or medicinal lotions, creams, ointments and anything else which may interfere with dressing adhesion at dressing application sites for the duration of the study from 24 hours before dressing application on Day 0. * Participant is willing to have excess hair removed from the dressing application sites * Participant is willing to avoid immersing the dressings in water (no swimming or bathing) for the duration of the study Footnote: \* at least 10% of participants are aged \>55 years Exclusion Criteria: * Female participant who is pregnant, or lactating. * Participant has a known sensitivity to any of the study products, materials or ancillary product or components. * Known skin sensitivity or allergies to adhesives, skin wipes, soap, surgical first-aid dressings, natural rubber or rubber latex, etc. * Participants with a current active skin disease (e.g., eczema, psoriasis, or severe dermatoporosis), sunburn or skin peeling at the dressing application sites. * Participants with a medical condi…