Container de stérilisation perforé (320x186x135mm) orange - Aygün - Delynov

What is the 320x186x135mm sterilization container with Teflon filters?

This device is an instrument sterilization box designed for the surgical environment. With precise dimensions of 320x186x135mm, it offers a volume suitable for storing complete instrument sets. Its structure is completed by an orange lid allowing for rapid differentiation of trays. The central technical element lies in the integration of Teflon filters, a material recognized for its thermal resistance and its ability to let steam pass through while blocking microorganisms. This dental surgery container is designed to withstand repeated autoclave cycles, thus ensuring the protection of the material against environmental contamination after the sterilization process.

What are the clinical indications for this container?

In oral, implant, or periodontal surgery, maintaining the asepsis chain is a fundamental requirement. This container is indicated for the organization of instruments necessary for invasive procedures. It allows for the grouping of tweezers, syndesmotomes, forceps, or drilling kits in a closed and secure environment. Its use is recommended for practitioners wishing to optimize the management of their sterile stock, avoiding the systematic use of disposable sterilization pouches for large volumes. It is perfectly suited for the prolonged storage of reusable medical devices between two interventions, guaranteeing that the instruments remain ready for use under optimal hygiene conditions.

What are the technical characteristics of this device?

The container has dimensions of 320mm in length, 186mm in width, and 135mm in height. Its design includes a high-performance filtration system using Teflon filters. Unlike single-use paper filters, Teflon offers increased durability and excellent water vapor permeability during the sterilization phase, while ensuring an effective microbial barrier during drying and storage. The orange lid facilitates selective sorting by type of procedure or by practitioner within a multi-practitioner structure. The closure is secured by robust lateral mechanisms, preventing any accidental opening during handling or transport between the decontamination area and the operating room.

What are the contraindications for the use of this container?

Although this container is versatile, it must not be used for the sterilization of devices incompatible with steam autoclave parameters (temperature and pressure). It is imperative not to overload the container beyond volume recommendations, as excessive instrument density can hinder steam circulation and compromise sterilization efficiency. The use of damaged, clogged, or poorly fixed filters constitutes a major contraindication to maintaining sterility. Finally, this device must not be used for the transport of unsealed biological waste or corrosive chemicals that could alter the integrity of the materials, particularly the seals and the Teflon filtration system.

What are the maintenance precautions to guarantee longevity?

To preserve the performance of this container, rigorous maintenance is necessary after each cycle. Cleaning must be carried out with pH-neutral detergent and disinfectant solutions to avoid corrosion of the surfaces. The condition of the Teflon filters should be inspected regularly to ensure the absence of perforations or premature wear. The seals located under the orange lid must remain clean and flexible to guarantee an airtight closure. When loading into the autoclave, the container must be positioned to promote the evacuation of condensate. Complete drying is essential before storage to prevent any risk of internal corrosion or bacterial development related to residual moisture.

Who is the manufacturer and what standards are respected?

This sterilization container comes from a manufacturing process specialized in medical-surgical instrumentation. Although specific certifications are not detailed here, this type of device is generally designed to meet the technical requirements of steam sterilization. The materials used, particularly for the container body and the Teflon filters, are selected for their biocompatibility and resistance to thermal stress. For any information relating to compliance standards, regulatory marking, or specific manufacturer instructions for use, it is imperative to refer to the technical notice and labeling provided with the product upon delivery.

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Surgical medical consumables play a decisive role in operative safety.