European standards

DERMEDICS™ offers medical gels, professional dermocosmetics and digital devices for aesthetic medicine treatments which are produced in accordance with European Union directives and standards:

Medical gels

  • They are registered in European Union as Medical Products Class I (Annex VII, rule 1) according to the Medical Device Directive 93/42/EEC.
  • The are manufactured according to Good Manufacturing Practices (GMP) and conform to ISO 13485:2012.
  • MSDS available on request.


  • Registered in European Union according to Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products (Text with EEA relevance).
  • They are manufactured according to Good Manufacturing Practices (GMP).
  • Not tested on animals.


  • All devices conform to Low Voltage Directive (LVD) 73/23/EEC+93/68/EEC and Electromagnetic compatibility (EMC) 89/336/EEC+92/31/EEC+93/68/EEC.
  • CE Declaration of Conformity available on request.

For further information please contact us directly.


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