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 European Union directives: The COUNCIL DIRECTIVE 93/42/EEC (MDD) and DIRECTIVE 2007/47/EC of The EUROPEAN PARLIAMENT and the EUROPEAN COUNCIL. 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 to illuminate such premises as: operating rooms, rooms designed for laparoscopic and endoscopic, surgeries and interventions, recovery rooms, dermatological offices and to illuminate blood collection centres, etc. Surface mounted luminary equipped in highly efficient LED sources. Luminary coffer made from steel sheet, powder coated in white. Screens and optical systems in aluminum frame. Accessories: electronic stabilizing and ignition system with possible light stream regulation. Emergency version available.