Stimulating excellence

Quality and Regulatory

We, at Neuromod Devices, are committed to delivering minimally invasive stimulation technologies to provide personalised treatments for people suffering with chronic neurological conditions.

Taking a risk-based approach, we maintain the effectiveness of our quality system to ensure responsiveness to customer needs while meeting applicable regulatory requirements.

Quality Management

Neuromod maintains a certified Quality Management System to to ensure compliance to the applicable regulations in regions that it distributes its devices.

Neuromod’s Quality System Certificate ISO 13485: 2016

Neuromod’s CE Certificate Full Quality Assurance

Product Conformity

Click on the links below for Neuromod’s Declaration of Conformity under the EU legislation governing medical devices.

Declaration of Conformity Medical Device Directive 93/42/EEC

Declaration of Conformity Radio Equipment Directive 2014/53/EU