Polyflon Technology is delighted to announce its eagerly anticipated accreditation to ISO 13485:2016, in association with BSI.
The certificate has been awarded to Polyflon for complying with the requirements of ISO 13485:2016 for the following scope; “the contract manufacture of non-sterile thermoformed polymer tube components for medical devices”.
Polyflon Medical, a specialist medical tube component manufacturing cell within Polyflon Technology Ltd., focuses on custom-made thermoformed medical tube components for single use, minimally invasive medical devices, produced, inspected and packaged at their Staffordshire, UK site.
Polyflon’s Quality Manager, Leanne Stubbings comments on the accreditation; “We’re so pleased to have been awarded this certification and we feel that implementing this standard is vital in demonstrating our commitment to quality.”
Polyflon’s Director, Matthew Pedley, adds; “This accreditation marks a milestone in our medical component manufacturing operation, and is a great start to 2024. We’re looking forward to accelerated growth with many new opportunities ahead.”
Article provided by Medilink Midlands Member Polyflon Technology, for more information click here.
