Quality Management at
Honer Medizin-Technik
A total quality management system ensures that all processes, from development to processing customer complaints, are controlled on a customer-oriented basis. This QA system is based on the EU legislation relating to medical devices and therefore fully complies with DIN EN ISO 13485:2003 requirements as well as with additional, internationally recognised standards pertaining to medical devices.
The monitoring of product quality at all stages of production from incoming materials, delivery to the final inspections is an indispensable part of our quality regulations. Our products are subjected to a 100% check at the end of their manufacturing process.
 
Quality Management:
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Certified quality management system in order of DIN EN ISO 13485 |
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Conformity Asessment of products in order of 93/42/EWG (CE) |
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FDA Registry |
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GMP (Good Manufacturing Practice) |
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