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Our ambition has always been the same: making it easier to help. Quality, safety and regulatory expertise are essential parts of how we turn that ambition into reality.
When First Aid products are needed, they need to be easy to use, safe and reliable. That is why quality and compliance are integrated throughout our entire product lifecycle — from product development and testing to manufacturing, documentation and continuous improvement. Designed in Sweden and shaped by more than 50 years of experience, Cederroth First Aid combines dedicated in-house innovation with quality and regulatory expertise. Our solutions help workplaces stay prepared for accidents and respond quickly when injuries occur.
From First Aid Stations and Eye Wash solutions to wound care, burn care and portable First Aid Kits, our products are developed for real workplaces and real situations.
We work systematically with product safety, usability, testing, risk assessment, documentation and traceability to help ensure that our products perform as intended when people need them most. These processes help ensure that our products are safe, reliable and ready to perform when needed.
The Medical Device Regulation (MDR) is the European Union’s regulatory framework for medical devices, introduced to strengthen requirements for product safety, performance, transparency and traceability. MDR helps ensure that medical devices are safe, perform as intended and can be traced throughout the supply chain. Manufacturers of Medical Devices of higher risk classes are regularly audited to ensure continued compliance with MDR requirements.
Cederroth First Aid is part of Orkla Health and Orkla Wound Care AB, an MDR-certified company. All Cederroth First Aid products manufactured by Orkla Wound Care AB of higher risk classes are included in our MDR certificate. This reflects our long-term commitment to product safety, quality and regulatory excellence.
Our quality management system is certified according to ISO 13485, the internationally recognised standard for quality management systems for medical devices.
Together with our MDR certification, this supports our commitment to product safety, quality and continuous improvement, providing confidence in First Aid solutions backed by documented quality, regulatory expertise and a strong focus on user safety.
Medical devices within the Cederroth First Aid range are CE-marked, demonstrating compliance with applicable requirements for medical devices within the European Union.
Download our current certifications related to quality management and regulatory compliance.
Certification of our quality management system for medical devices according to ISO 13485.
Download certificate
Certification demonstrating compliance with the European Medical Device Regulation (EU) 2017/745.