Cleanroom production
Sensitive electronics demand more than precise assembly, they require environments free from contamination.
At EPSa, modules and systems are assembled, tested, and packaged in fully air-conditioned clean rooms, including facilities certified to ISO Class 5. These controlled conditions ensure extremely low failure rates and guarantee long-term functional reliability.
For critical applications
Cleanroom production is essential for markets such as medical technology, where the smallest disturbance can compromise performance.
Our specially trained teams follow strict protocols to minimize airborne particles, eliminate interference factors, and meet all relevant quality standards. This provides the assurance that your products function reliably, even under challenging conditions such as vibrations, electrical interference, or ionizing radiation.
Key capabilities:
- ISO Class 5 clean room facilities
- Fully air-conditioned clean room environments
- Assembly, testing, and packaging under controlled conditions
- Manufacturing compliant with DIN EN ISO 13485 for medical devices
- Preventive reduction of airborne particles
- Maximum functional reliability with minimized error rates
- Cost savings through reduced rework.
