Successful DEKRA Surveillance Audit according to ISO 13485

We are pleased to announce that Silcoplast has successfully passed the DEKRA surveillance audit in accordance with ISO 13485, the internationally recognized quality management standard for medical devices.

The audit once again confirms the effectiveness of our quality management system and our commitment to maintaining the highest standards in processes, products, and services. ISO 13485 ensures consistent compliance with regulatory requirements and supports the delivery of safe and reliable medical device components.

This successful audit outcome provides further assurance to our customers and partners that quality, safety, and reliability remain top priorities at Silcoplast. It also reflects the dedication and professionalism of our entire team.

We would like to thank all employees whose commitment contributed to this achievement and look forward to continuing our pursuit of excellence in quality and customer satisfaction.