Centre d'expertise en retraitement des dispositifs médicaux

This document is intended for managers and clinical personnel involved in medical device reprocessing (MDR).

Its purpose is to describe the guidelines to be followed for the overall process of collecting, disinfecting and storing single-use N95 FFRs in order to:

This document is intended for decision makers, managers and clinical personnel involved in medical device reprocessing (MDR). It presents the technologies approved by Health Canada in the COVID-19 context as well as a promising - although as yet unauthorized - option for disinfecting N95 FFRs.

The present document analyzes current knowledge about available disinfection options for N95 FFRs and puts into perspective the advantages and limitations of each disinfection process identified. The authorizations that have been issued by Health Canada are also specified. Finally, the recommendations of the CERDM are presented.

This professional practice guide is a basic reference on the quality of water used for reusable medical devices reprocessing (MDR) and flexible endoscopic devices reprocessing (EDR). It aims to support activity management, to standardize practices and to improve the quality of MDR. It is intended for all persons working in health care institutions who are directly or indirectly responsible for quality assurance in MDR, including managers, MDR institution respondents, MDR staff, and persons…

The frequency of adverse events (incidents and accidents) related to medical device reprocessing (MDR) is a concern for health care services. By definition, an incident means that a medical device breaches a recognized standard for MDR without having been used on a patient. An accident refers to any use on a patient of a medical device which does not meet a recognized standard for MDR, with that use potentially affecting the patient’s health status (INSPQ, 2014).

This report…