Compliance
DermMedica supports informed purchasing by providing documentation tied to the exact device, configuration, intended use, and destination.
Regulatory status, indications, labeling, and required operator qualifications may differ by device model, configuration, and jurisdiction. Buyers should request and review the documentation applicable to the exact system quoted.
A statement about one component, technology, or model must not be interpreted as applying to every DermMedica product. DermMedica will provide available model-specific regulatory information during the professional sales process.
Professional aesthetic devices must be used only by appropriately trained and authorized personnel. The purchaser is responsible for confirming licensing, medical-director, facility, supervision, and treatment requirements in the location where the device will be operated.
Contact dermmedica.sales@gmail.com with the exact product name and intended location of use to request available specifications, labeling, warranty information, and regulatory documentation before purchase.
Tell us the model and where it will be used so our team can provide the relevant available materials.
Request Documentation