ISO 9001:2015 Quality Management System is a globally accepted form of a quality management system that aims to increase customer satisfaction by meeting customer expectations, needs, and regulatory requirements.
Dental Abutment CE Certificate
(The 93/42/EEC Medical Device Directive is an international standard that contains special requirements for medical devices. ISO 13485 is one of the most important arguments that medical device manufacturers can use when going for CE Marking. If the production quality assurance module is selected within the scope of CE Marking, it is a requirement for companies to establish. is the system.
Quality Management System
ISO 13485:2016 Medical Devices Quality Management System is a globally accepted standard that has been specially prepared for the medical device industry, meets the specific requirements of an organization as well as legal regulations, and demonstrates its competence in the production of medical devices and related services.
Machinery CE Certificate
(2006/42/EC Machinery Directive)
Machine CE Certificate is the machine; It is a document proving that it has been produced in a way that will protect human and environmental health in its production, installation, and use, with its technical file ready and tested.