REGISTERED MEDICAL DEVICE
Dermalize Protective Tattoo Film is made of polyurethane and hypoallergenic acrylic glue and it is registered as a medical device of class I with the Italian Ministry of Health (Reg.1338731/R e 1338737/R), as well as with the American FDA (Food & Drugs Administration).
It is dermatologically tested and before its release on the global market in February 2015, it had been tested for about 2 years by a pool of 10 among the most qualified and renown tattoo artists in the world.
Dermalize (D-lizepro in the USA) sets itself on the global tattoo market as a certified medical replacement of the commonly used alimentary cling film. The film is breathable, letting oxygen in and allowing excess moisture vapor to be released from the wound.
It builds an antibacterial barrier that guarantees a thorough protection from external agents. The tattoo film must be changed regularly as prescribed on the “How to use” section.