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      We support medical-technology companies in all aspects of certification according to DIN EN ISO 13485 / MDR 2017 / MDD. To this end we efficiently create all necessary documentation such as the Quality Manual, Technical Documentation and Risk Management.
      QM consulting
      • QM-Consulting / Certification
      • Quality Management System
      • Technical documentation
      • Validation of Processes
      • Reprocessing Validation
    • Sourcing

      We are an excellent partner for the procurement, development and manufactur of surgical instruments for highest quality requirements. With our technical expertise we are pleased to do your project management, providing documentation for all the required standards.
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      • Technical quality control
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Certificate DIN EN ISO 13485:2016

 

Certificate Annex V

MEDITEC SOURCE GmbH & Co. KG

Sattlerstraße 19
78532 Tuttlingen

Tel. +49 (0) 7461-90827-0

 

 

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