Update your documentation before MDR

We are rapidly approaching May 2020, and the deadline for full introduction of MDR 2017/745, The EU Medical Devices Regulation.

As an accredited test lab, NIOM can offer a confidential third-party evaluation of your dental materials. Wether you seek to re-certify products according to the current requirements, or get evaulated according to the new MDR, NIOM can be your trusted partner for materials testing.

NIOM has almost 50 years of experience in testing and evaluation of dental materials, first as the sole certifier for the Nordic certification program for dental materials. Since 1992, we have been an accredited laboratory (ISO/IEC 17025) within the field of dentistry.

Your testing needs
The focus of NIOM’s staff is research and testing of dental biomaterials. We always seek to increase our knowledge and develop in-house and international methods for robust investigation of biomaterials.

NIOM’s accredited methods cover all types of materials and a vast variation of characterizations, from in vitro cytotoxicity to physical properties. Among our expertise, you find testing of restorative materials, e.g. composites, cements, bonding agents and endodontic materials, as well as prosthetic materials, e.g. denture and orthodontic base materials, ceramics, metal sub-structures, and impression materials.

Our experts
NIOM scientists are appointed experts in the standardization of dental materials, both internationally (ISO TC 106 Dentistry) and in Europe (CEN TC 55 Dentistry). Thus, we are always up to date with the developments and requirements within standardization of dental materials.

NIOM offers a confidential third-party evaluation of your dental materials for the compliance with the current requirements.

Get in touch at niom@niom.no for more information and a quotation for our technical assistance. 

NIOM Newsletter for clients and partners Q3 2019