Articles of Interest
How to select sterile barrier systems for reusable medical device Publised by Chris Newmarker at Medical Design And Outsourcing.
ASISTHOS RECERTIFICA ISO 9001:2015 23 de marzo del 2018, Por Dr. Gustavo Luis Enriquez, Director Técnico de Asisthos S.R.L
How to select sterile barrier systems for reusable medical device Publised by Chris Newmarker at Medical Design And Outsourcing.November 14, 2017 .
AAMI Publishes New Sterilization Standards (Published by AMMI at AAMI News December 2017)
Considerations for Sterilization and Biocompatibility of 3D Printed Orthopedic Devices Posted in Orthopedics by MDDI Staff on October 10, 2016
How to choose a contract sterilization vendor Posted in Sterilization Services by Jamie Hartford, 30 de julio de 2014
Evaluation of the sterility maintenance of wet materials after steam sterilization and after 30 days of storage. (Source: Rev. Latino-Am. Enfermagem vol.18 no.4 Ribeirão Preto July / Aug. 2010).
The Cost of Package Integrity (Originally Published by MDDI in October 2005)
Reduction of bioburden in critical points througout the process. A fundamental step for the implementation of a HACCP process.
Optimization of packaging design for ethylene oxide sterilization. An ethylene oxide (EtO) sterilized medical device must be sealed in a carefully designed gas-permeable package that enables the EtO gas to enter...
Ethylene oxide sterilization: An introduction to the process. Ethylene oxide, or ethoxycyclopropane, is widely used in its pure state or in variable mixtures as a sterilizing agent at low temperatures.