Peracetic Acid Endoscopy Disinfectants designed and manufactured within an accredited ISO 13485:2016 Quality
Management System and CE marked.
With BSI as our notified body, we manufacture type tested disinfectants in our manufacturing facility in Yorkshire, England.
We supply decontamination facilities across the country with their AED approved chemistry, by choosing a chemistry
manufactured in the UK, Trusts can add to their ongoing environmental targets and carbon footprint reduction by selecting UK manufactured rather than imported chemistry.
A devotion to quality and patient safety forms the core of all we do, iM Med is proud to hold the ISO 13485: 2016 accreditation.
The ISO 13485 standard is an effective solution to meet the comprehensive requirements for a Quality Management System.
Adopting ISO 13485 provides a practical foundation for manufacturers to address the Medical Device Directives, regulations and responsibilities as well as demonstrating a
commitment to the safety and quality of medical devices.
Compliance with EU MDR regulations is essential for ensuring patient safety and minimising risks associated with medical devices and chemicals used in healthcare.
iM Med has successfully completed the transition process to EU MDR certification.
iM Med has held UKCA certification since November 2022 and therefore are now able to mark our products in compliance with both the UK and EU MDR regulations.
iM Med is proud to be a carbon neutral business >
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