DERMEO QUALITY

DERMEO et son contrôle qualité

Abides by regulatory and medical requirements

DERMEO is part of a dynamic progress at the cutting edge of technology and brings the expertise of certified bodies ISO 9001 and ISO 13485. ISO 9001 relates to the quality of management and systems and ISO 13485 specifies the requirements for quality of management and systems for the medical device industry. Compliance with these individual international organizational standards and medical services by DERMEO is a guarantee of quality for its customers and suppliers.

Quality controlled, safety checked

AFFSSSAPS FDA

SANTE CANADA - HEALTH CANADA DERMEO AUSTRALIA GOVERNMENT

Evolutionary technology

DERMEO medical devices with pulsed light are the first French medical CE class IIb marked devices in accordance with applicable regulations. This level of regulation requires the intervention of a body authorized by the European Commission to audit the quality of DERMEO products and services.

Markings and International Healthcare approvals

DERMEO has received the CE mark and AFSSAPS approval and numerous ministries of health around the world, including the FDA (Food and Drug Administration) for the United States and the Ministry of Health Canada which proves the effectiveness and safety of DERMEO medical devices.

INTERTEK

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