To demonstrate our technical commitment to excellence we abide by the most stringent medical guidelines.
Operating in accordance with The Medical Device Directive. Steroplast work to the guidelines of BS EN ISO 13485:2016 supported by: The Medical Device Directive (M.D.D.) 93/42/EEC: and our Wholesale Dealers of Licence.
Our "Quality Assurance System" is there for your peace of mind and is maintained under the supervision of our notified body: S.G.S. All our products are supported by our quality system which ensures compliance with the *Medicines & Healthcare products Regulatory Agency (M.H.R.A.)
Supplier Ethical Data Exchange (SEDEX)
As members of SEDEX, it demonstrates we are an organisation committed to continuous improvement within our ethical supply chains.
How our CE mark benefits you:
All Steroplast medical devices carry the CE mark. This is our 100% guarantee that through our internal quality assurance department and the *M.H.R.A. all our products exceed all E.U. standards.
We are happy to be one of the 4500 members of the Greater Manchester Chamber of Commerce, which offers business support to companies in the Greater Manchester area.
Steroplast is part of the British and Irish Trading Alliance.