Final answer:
Implements must be immersed in a disinfectant approved by the FDA and EPA. Use-dilution tests validated by the AOAC or similar organizations ensure the disinfectant's effectiveness. Safety protocols must be strictly followed to ensure the health and safety of personnel and patients.
Step-by-step explanation:
All implements must be immersed in a disinfectant approved by government agencies and regulatory bodies such as the Food and Drug Administration (FDA) and the Environmental Protection Agency (EPA). Agencies like the FDA provide protocols for the disinfection and sterilization of medical devices. Additionally, disinfectant solutions must be tested to ensure efficacy. This is typically carried out using the use-dilution test, which measures a chemical agent's effectiveness against specific microorganisms on inanimate surfaces. It is essential that these disinfectants are effective, stable, inexpensive, and meet the rigorous criteria imposed by regulatory agencies to protect public health.
Disinfectant manufactures also have to perform use-dilution tests that are validated by organizations such as the Association of Official Agricultural Chemists International (AOAC). The AOAC defines standards to ensure that a disinfectant remains effective when used accurately and consistently in clinical environments. Personal protective equipment such as coats, gloves, and face protection is crucial for personnel handling contaminated material, and strong basic solutions like 1 N NaOH may be required for decontamination.