Aesculap SterilContainer System: Instructions for Use

Overview of the SterilContainer System

This document provides comprehensive instructions for the Aesculap® SterilContainer™ System. It details the system's components, proper usage, decontamination, cleaning, inspection, and assembly procedures. The guide covers various sterilization modalities, including Steam, Ethylene Oxide, and Vapor Hydrogen Peroxide (e.g., STERRAD®, STERIS® V-PRO®, STERIZONE®).

Key Information Provided

• Detailed guidance on preparing and using the SterilContainer System.
• Specific sterilization cycle parameters for different modalities.
• Information on compatible accessories, filters, locks, and indicator cards.
• Validation testing summaries and FDA clearance information.
• Procedures for inspection, maintenance, and aseptic presentation.

Purpose and Scope

The primary purpose of this guide is to ensure the effective and safe reprocessing of surgical instruments using the Aesculap SterilContainer System. It serves as a critical resource for healthcare professionals involved in sterile processing.