We manufacture medical devices for dermatological and aesthetic use in compliance with Regulation (EU) 2017/745 (MDR). We offer a complete service, from the classification of the medical device to the development of the technical file for obtaining the CE marking.

Included services:

• Specific formulation for DM Class I, IIa, IIb
• Technical documentation and CE certifications
• Compliant labeling and audit support
• Traceability management and quality system

Trust ENOVA SWISS for a safe, compliant, and competitive private label.