Container de stérilisation 320x186x135mm avec filtres Téflon - Couvercle Brun - Delynov (Aygün)

What is the 315x133x70mm sterilization container with Teflon filters?

This sterilization container is an instrumentation management device designed for surgical environments. With precise dimensions of 315x133x70mm, it offers a volume suitable for packaging specific instrument sets. Its structure is completed by a distinctive black lid and an advanced filtration system. Unlike single-use systems, this model integrates Teflon filters, recognized for their durability and resistance to repeated steam sterilization cycles. This surgical sterilization box is designed to protect instruments against external contamination while allowing effective penetration of the sterilizing agent, thus guaranteeing the integrity of the equipment until its clinical use.

What are the clinical indications for this device?

This container is indicated for the sterile processing of instrumentation used during oral surgery, implantology, periodontology, and maxillofacial surgery interventions. In clinical practice, it serves as a sterile barrier for implantology drills, syndesmotomes, bone forceps, or any other surgical instrument requiring rigorous decontamination in an autoclave. Its use allows for the organization of technical trays by type of intervention, thus facilitating the workflow within the operating room. It ensures the secure transport of soiled instruments to the decontamination area, followed by their storage after sterilization, maintaining the sterile state until the lid is opened during the surgical act.

What are the technical characteristics of this sterilization container?

The container features dimensions of 315mm in length, 133mm in width, and 70mm in height, which classifies it among the compact formats suitable for standard dental practice autoclaves. Its main technical characteristic lies in the integration of Teflon filters. These permanent filters eliminate the need for disposable paper filters, offering a more durable and stable solution in the face of high temperatures. The black-colored lid allows for immediate chromatic differentiation, useful for separating surgery kits (e.g., extraction kit vs. implant placement kit). The design of the tub and lid ensures optimal sealing once locked, protecting the contents against microorganisms after the drying phase.

What are the contraindications for the use of this container?

There is no direct medical contraindication related to the use of this surgical sterilization container, as it does not come into direct contact with the patient. However, technical contraindications apply: it must not be used with sterilization methods incompatible with its materials, such as dry heat (poupinel) if the gaskets or filters are not specifically designed for this purpose. Furthermore, the use of highly corrosive cleaning products or those not complying with recommendations for metal alloys and Teflon can compromise the integrity of the device. It is imperative not to overload the container, as excessive crowding can prevent correct steam circulation and compromise the sterility of the contents.

What are the maintenance precautions to guarantee the longevity of the Teflon filters?

Maintenance of this dental sterilization container relies mainly on the regular inspection of the Teflon filters and the sealing gaskets. Although Teflon filters are designed for prolonged use, they must be checked after each cycle to ensure the absence of perforations or residues obstructing the pores. Cleaning must be performed with pH-neutral solutions to avoid oxidation of the walls or degradation of the components. It is recommended to scrupulously follow the autoclave drying cycles to avoid any accumulation of residual moisture inside the container, which could promote long-term corrosion or contamination during storage. Storage in a dry and dust-free place is essential.

Who is the manufacturer and what standards are respected?

This product is manufactured according to rigorous quality standards to meet the requirements of healthcare professionals. Although specific certifications (such as the regulatory class or CE marking) are not detailed in the current source data, this type of device is generally designed to comply with current hospital and dental sterilization protocols. The materials used are selected for their indirect biocompatibility and thermal resistance. To obtain precise information on compliance standards, ISO certifications, or the specific CE marking for this container model, it is necessary to systematically refer to the instructions for use and technical documents provided by the manufacturer at the time of purchase.

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Surgical medical consumables play a decisive role in operative safety.