CE marking indicates that a product has been assessed by the manufacturer and deemed to meet EU safety, health and environmental protection requirements. It is required for products manufactured anywhere in the world that are then marketed in the EU.

The assessment criteria and requirements depend on the risk level and complexity of the device, so manufacturers must determine whether their device is covered by the MDD or another directive (for example, the Active Implantable Medical Device Directive).

The BSI Kitemark™ is a quality mark owned and operated by BSI.

With UKAS accreditation – benefits include risk reduction, increased customer satisfaction and access to new customers around the world.

UL Listing means that UL has tested representative samples of a product and determined that the product meets specific, defined requirements. These requirements are often based on UL’s published and nationally recognized Standards for Safety.