ISO 13485 Certified
Production
ISO 13485 is the internationally accepted standard a medical device organization can implement to demonstrate compliance with MedTech legislations. Adopting ISO 13485 provides a practical foundation for manufacturers to address the regulations and responsibilities as well as demonstrating a commitment to the safety and quality of medical devices.
EvidenceUltra-Fresh
Production
All Dunlop Foams products are treated with Ultra-Fresh – an antimicrobial treatment which helps control dust mites and other household bugs that trigger allergies and asthma. It also helps keep foam cleaner and fresher for longer by controlling bad and unwanted odours caused by bacterial growth. Ultra-Fresh was created more than 60 years ago in Canada and is now used in over 50 countries by 500+ manufacturers.
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