Intertek Medical Notified Body (IMNB); Now designated under Medical Device Regulation (MDR) 2017/745

WHAT DOES THIS MEAN?

Intertek Medical Notified Body now can start the process of taking on applications for MDR certification.

 

 WHO CAN APPLY?

Our current MDD clients and new clients can apply. Please ensure the codes covering your products are part of our scope of designation. Our scope of designation can be found on the NANDO webpage here.

 

 

 HOW DO I APPLY?

The MDR application process describes the basic step by step process of what to do and what to expect during our application process for MDR.

 

WHAT HAPPENS NEXT?

The pre-application form needs* to be completed before we start the formal application process for MDR.

 *This is optional for our current clients under MDD, please contact us at IMNB@intertek.com for more information.

 HOW ARE CLIENTS PRIORITISED?

Intertek Medical Notified Body will take on MDR clients on a first-come, first-served basis, with priority given to current MDD clients.

 

COMPLETE THE PRE-APPLICATION FORM

 

Auditing and System Certification Services

 
 
 
 

MDR Application Information

Process Chart IMNB - Application Procedure for Clients
IMNB MDR Application Process Presentation
IMNB MDR Impartiality Procedure
IMNB MDR List of Standard Fees 2020
IMNB Process for Changes in Certification Status