POLICIES & CERTIFICATES

Legal information and resources

Policies

Cookies policy

Code of conduct

Prevention of money laundering policy and compliance with international sanction policy

Data processing agreement

Teltonika terms of service

Recruitment data policy

Integrated management system policy

Warranty & repair

Certificates

ISO 9001:2015 Quality service certification

ISO 14001:2015 Environmental system certification

ISO 45001:2018 Safety system certification

ISO 27001:2022 Information security management system

ISO 13485:2016 Quality system certification

Updated 2025-03-01

ISO 13485 is the standard created to ensures the consistent design, development, production, installation and delivery through to disposal of medical devices that are safe for their intended purpose. This standard allows to reduce safety and legal risks while creating more economical work environments. As an internationally recognized standard of quality and safety for medical device manufacturing, having ISO 13485 certification helps be recognized as more reputable, trustworthy partners.