Gen 2 Battrode Wear Study

Inclusion criteria

• Participant is ≥ 18 years.
• Completes the consent process as required.
• Participants can speak and read English fluently.
• Willing to allow shaving of device application area, as required.
• Willing to take photos of the application area before wear, daily during wear, and immediately after removal.
• Willingness to report current known pregnancy.

Exclusion criteria

• Unable to comply with the study protocol and instructions for wearing the devices for up to 15 days.
• Any pre-existing breached or compromised skin, skin rash, irritation or infection at the application area.
• Any incision, wound or scar in the application area.
• Participants with known skin allergies and sensitivities to adhesives.
• Participants with scheduled electronic imaging (including magnetic resonance imaging), cardioversion, and/or procedures where device would be removed during the data collection period.
• Participants with known history of cardiac arrhythmias.
• Participants with chest anatomies not compatible with secure parasternal placement.
• Use of clothing or garment that can dislodge or loosen the patch or bras with underwires or other worn items that might interfere with the devices under study.