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In 2003, the MESO GbR management decided to implement an internationally accepted quality management system.
The MESO group was recertified in October 2009. |
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The quality management system of the MESO group takes into account the following standards.:
DIN-EN-ISO ISO 9001:2000,
DIN-EN-ISO ISO 13485:2003
Provisions of the VBG and for technical documentation
To view our QMS-Handook, click on Download. |
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All MESO products are in full compliance with the Essential Requirements of the European Medical Device Directive 93/42/EEC.
To view our CE Conformance Statement, click on Download. |
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The company's quality managment system according to ISO 9001:2000
and ISO 13485:2003 (medical products) serves to guarantee that general qualitystandards as well as the particularly high standards set for the production of medical device are fully complied with in every-day work.
To view our quality management system certificate,
click on Download. |
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