7/30/2023 0 Comments Cerec bluecam prismatic tube lens![]() Food and Drug Administration (FDA) has approved both the CEREC Omnicam and CEREC Bluecam as reusable Class II Medical Devices. The CDC “Guidelines for Infection Control in Dental Health-Care Settings” recommends sterilization for critical devices, high-level disinfection but preferably sterilization for semi-critical devices, and cleaning with low-level disinfection for noncritical devices. Noncritical device - touches only intact skin and not mucous membranes Semi-critical device - will contact non-intact skin or mucous membranes but will not penetrate them Angle-right In the United States, the Centers for Disease Control and Prevention (CDC) uses the Spaulding Classification to stratify medical devices into three categories intended to guide healthcare professionals on the best method to reprocess reusable medical devices.1 The classification is as follows: Angle-rightĬritical device - will enter sterile tissue, including the vascular system Angle-right As new developments in digital technology continue to influence dental treatment, it is a good time to review the current recommended procedures for use of the CEREC® Omnicam and CEREC Bluecam. Recently, several highly publicized events related to medical device disinfection and sterilization have appeared in the news, reminding both patients and providers that it is essential to have validated and consistent protocols in place to prevent crosscontamination between patients. CEREC - Q3 2018 Prevention Of Patient Cross-Contamination With CEREC® Camerasĭennis J. ![]()
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