MDRAO Practice Exam 2025 – Complete Exam Prep Resource

Critical medical devices, such as biopsy forceps, are characterized by their use in invasive procedures where they come into direct contact with sterile tissues and fluids. Because of this high-risk application, it is essential that they undergo thorough sterilization to eliminate any potential pathogens. The sterilization process ensures that all microorganisms, including bacteria, viruses, and spores, are eradicated, thereby minimizing the risk of infection to the patient.

In the case of critical devices, the standard practice is to sterilize after each use to maintain safety and compliance with health regulations. Simply monitoring these devices or claiming they can be reused without sterilization poses significant risks and fails to adhere to established infection control protocols. Therefore, the requirement for sterilization is a fundamental characteristic of critical medical devices, ensuring patient safety and promoting optimal clinical outcomes.