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An ideal combination that is much more compact than before: the automation system CPX-E and the valve terminal VTUG together in a control cabinet. This is a complete solution that is easy to install and keeps tubing installation to a minimum.

• Use, storage and transport conditions for Festo products
• Standards in pneumatics
• Compressed air preparation
• Operating conditions for valves
• Port designations of pneumatic components to ISO 5599
• Operating conditions for drives
• Pressure/force table and graphBuckling load graph
• Air consumption
• Pneumatics and explosion protection – ATEX
• EC directives/approvals
• Design – Clean room suitability
• Paint-wetting impairment substances and resistance to media
• Corrosion resistance class CRC
• Protection classes according to IEC/EN 60529
• Functional earth – protective earth – PELV
• Spark arresting

Our drive solutions for controlling dampers for all industrial sectors in which processes are operated with gas, oil, coal or biomass, and the air supply must be extremely precisely and reliably controlled.

Automation for the requirements

in the process industry

Previously being our Focus Product brochure, Festo North America presents our Key Products for North America brochure.  This brochure stars our key product for the year pertinent to the North American Region.

The advent of digital pneumatics promises to change how machines and processes are designed and managed throughout the industrial world. It’s a technological disrupter with exciting potential applications in oil and gas exploration and production.

Automation World, August 2016

RSC Mason obtained certification under the ISO 13485:2016 standard on January 24, 2023. This standard sets forth the requirements for a Quality Management System (QMS) in the design and manufacturing of medical devices. To achieve certification, an organization's QMS must successfully pass a third-party Medical Device Single Audit Program (MDSAP) Audit. This certification ensures that Festo can consistently provide medical devices and related services that meet both customer expectations and any relevant regulatory requirements, by demonstrating its ability to implement a QMS. Ultimately, the goal is to generate qualified leads from customers who require products for the production of medical devices.

The ongoing need to make process adjustments in modern automation systems opens itself up to unwanted device tampering. This white paper outlines a five-step process to ensure effective, error-free process adjustments of pneumatic components.