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QA, QM and Quality standards

The use of computer-aided production based on the latest technology ensures a high precision standard. The clean-room production of medical devices is according to tightest quality criteria of DIN EN ISO 13485:2012 which is attained by consequent record of work, monitoring and evaluation of work and control process data. Our quality management program and the quality assurance is the base for the regular certification of our QM-system. In order to assure the demand of premium quality and traceability, the used raw materials are selected by strict quality criteria and regular in-process controls are performed during the production process.

Long-term experience combined with a consequent quality management grant the safety and reliability of our products, the dialogue with our customers ensures a continuous innovation of the existing product range and practical-aligned solutions.


Zertifiziert nach
EN ISO 13485:2016