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.)
In alignment with our commitment to safety and ethical business practices, Steroplast Healthcare has partnered with TINYg, a global non-profit organisation devoted to the prevention of terrorism and enhancing security. This collaboration underscores our dedication to contributing positively to community safety and well-being.
By working with TINYg, we extend our commitment beyond healthcare, supporting initiatives that provide valuable information and resources to professionals in various sectors, including corporations, law enforcement, and academia.
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.