BIOMATCAN Ltd. Achieves ISO 13485 Certification for Medical Devices

News release from BIOMATCAN Inc. Jenn O'Donnell September 8, 2017

BIOMATCAN LTD is very pleased to announce that it has become ISO 13485 certified.

The certification issued by the leading international provider of quality management systems and their certification, INTERTEK, attests that BIOMATCAN’s Quality Management System for Medical Devices responds to rigorous standards for the design and development, manufacturing, packaging and distribution of synthetic bone filler and bone substitute for bone regeneration.

The achievement of this important objective is a key step toward the global marketing of the company’s products.

ISO 13485 establishes the requirements of a quality management system whereby an organization must demonstrate its ability to consistently provide medical devices and associated services that meet the requirements of customers, as well as meeting applicable regulatory requirements for medical devices and associated services.

BIOMATCAN Chief Operating Officer, Fouad Dabbarh


BIOMATCAN Ltd. is a unique Canadian company specializing in the Research, Development and Commercialization of innovative biomaterial products for the orthopedic and dental applications worldwide.

For more information please contact:

Email: , Tel: 506 450-0404, Fax: 506 450-0405, Unit#3, 385 Wilsey Road  Fredericton, New Brunswick, Canada

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