We, the management of the MESO group, commit ourselves to realize an active and continuously improving quality management system (QMS).
The MESO group consistently follows stringent quality requirements to ensure a high product quality. The development of complex medical software and hardware underlies specific criterias concerning test and evaluation. During the development and test phase each step is documented and reproducible.
We continually review and enhance our QM system to improve its quality. Our corporate mission and our strict quality objectives are the basis for our daily work.
In December 2018 the MESO group has been successfully recertified.
The MESO group is certified according medical product norm EN ISO 13485:2016.
Since 2013, meso international GmbH owns the certification DE AEOF 118936 as Authorised Economic Operator.
All MESO products are in accordance with the Medical Devices Act (Medizinproduktegesetz MPG) and fulfill the requirements of the European guideline for medical devices 93/42/EEC.