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Processes, Mechanical Engineering, Manufacturing & Automation
Speak with our exhibitors and discover how they can help you in the processes involved in medical device production.
Processes, Mechanical Engineering, Manufacturing & Automation
Biomedical engineering is subject to the standard DIN EN ISO 13485:2016. This norm lays out the requirements for quality management systems covering medical device design, development, manufacture, installation and maintenance. Machinery used in medical device manufacturing must offer a high degree of precision and reliability. These requirements became even more demanding with the European Medical Devices Regulation (MDR). Medical device manufacturers must also pay attention to quality management for outsourced processes.
Speak with our exhibitors and discover how they can help you in the processes involved in medical device production:
- Surface functionalisation / treatment
- Metal processing
- Plastic processing
- Processing of ceramics, glass and composites
- Additive manufacturing
- Robot systems, automation
- Laser processing
- Tool production and mould making
- Extrusion
- Sterilisation
- Clean room
- Contract manufacturing
- OEM
- Packaging and packaging technology
- Printing, bar coding, labelling
Do you have any questions? Please contact us
MedtecLIVE Sales-Team
Jessica Nether and Silke Ludwig
We will be glad to advise you.
medteclive@