This product is manufactured in production plant which holds quality management system for medical devices ISO 13485. Moreover, the product is consistent with fundamental requirements defined in the directive 93/42/EWG. In Poland the product fulfils the requirements defined in the Act of May 20th 2010 of MEDICAL DEVICES and is declared and registered in OFFICE FOR REGISTRATION OF MEDICAL PRODUCTS, MEDICAL DEVICES AND BIOCIDAL PRODUCTS. Luminary is recommended to be used in medical sector for installations in hospital wards.