As a manufacturer of medical devices, we meet the strictest quality requirements set by ISO 13485. The company has an established quality management system where every employee of our company is part of this system.
Product safety and quality has been our priority since the beginning of the company. In 1995, we were the first company engaged in the production of implants and instruments for orthopaedics and traumatology in the Czech Republic to obtain ISO:9001 certification from the independent German certification company RW TÜV Essen.
Our company complies with the European Union directive 93/42/EEC and has CE certification for medical devices I, IIb and III.
BEZNOSKA s.r.o. is constantly working on improving the quality of its products and continuously improving its processes. Currently, the process of transition to the EU Regulation 2017/745 is underway.
Ing. Jan Rouček - Head of Quality Management
Ing. Petr Mračno - Quality Officer
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© 2021 BEZNOSKA, s.r.o.