Certification
Accredited certification services for hearing and respiratory PPE, helping you meet global regulatory requirements and demonstrate product compliance.
Expert Guidance
Our team of experts provides tailored support, ensuring your products meet all necessary regulations and applicable standards for market approval.
We can offer a comprehensive range of EU Notified Body services for PPE manufacturers aiming to place their products on the European market.
Our approval scope covers various protection capabilities, including defense against cold, heat, electric shock, biological agents, chemicals, mechanical risks, slipping, and static electricity.
Manufacturers, suppliers, and buyers can leverage Eurofins Electrical & Electronics’ extensive network to ensure smooth, compliant market access with CE Marking.
Regulation (EU) 2016/425 governs PPE sales in the European market. It defines three categories:
For Category II and III PPE, manufacturers must conduct product testing at accredited laboratories and submit CE Marking requests to a Notified Body. For Category III products, an annual review via factory audit or sample testing is required.
Navigating complex EU regulations for hearing and respiratory PPE can delay market access.
We simplify EU market access with accredited certification for hearing and respiratory PPE, ensuring compliance with regulations and faster approval for your products.
Connect with our experts today and let us help you deliver compliant, safe and certified products to your markets.