Sanatmetal Ltd. obtained a certificate of compliance with the ISO 9001 standard in 1995. From 1997 our company is licensed to use the CE mark for its whole product range. From 2005 Sanatmetal operates an integrated management system which includes the quality management and environment management systems.
The commitment toward quality and continuous improvement is also proved by winning the National Quality Award in small companies category.
All processes of the company including product development, quality management, production, packaging process, handling of partners comply with the requirements of the ISO 9001, ISO 14001, ISO 13485 standards, Medical Device Directive 93/42/EEC together with the 4/2009 (III.17.) order of Ministry of Health, besides meeting the relevant legal requirements.
The Notified Body of the Sanatmetal Ltd. is the British Standard Institution (Notified Body No. 0086) which regularly controls and supervises the whole management system twice a year. Furthermore, product development and the cleaning process are controlled on special technical, microbiological and environment management audits. Our environmental management system is certified by Mert-Cert.
In 2008 the company obtained the FDA registration for intramedullary products. All the related activities are managed by Organix Llc in the USA.
The FDA approval is downloadable here: FDA approval.pdf
The Notified body of SanatSwing knee prosthesis and the Pannon and Sanat hip prosthesis systems is the EMKI (Notified Body No. 1011). According to the valid new regulation this product range belongs to class III and its authorization process was carried out accordingly.
The printable version can be downloaded here: Certificates.pdf
In 2014 ANVISA audited the activity and quality management system of Sanatmetal and the compliance with Brazilian rdc16/2013 GMP regulations. The printable version can be downloaded here: ANVISA Certificate