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 adapted for the packaging of 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 ensuring 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 procedures. In clinical practice, it serves as a sterile barrier for implantology drills, syndesmotomes, bone rongeurs, or any other surgical instrument requiring rigorous decontamination in an autoclave. Its use allows for the organization of surgical trays by type of intervention, thus facilitating the workflow within the operating theatre. It ensures the secure transport of soiled instruments to the decontamination area, and their subsequent storage after sterilization, maintaining the sterile state until the lid is opened during the surgical procedure.

What are the technical characteristics of this sterilization container?

The container measures 315mm in length, 133mm in width, and 70mm in height, classifying it among the compact formats suitable for standard dental surgery autoclaves. Its main technical feature lies in the integration of Teflon filters. These permanent filters eliminate the need for disposable paper filters, providing a more durable and stable solution against high temperatures. The black 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 micro-organisms after the drying phase.

What are the contraindications for the use of this container?

There are no direct medical contraindications related to the use of this oral surgery 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 seals 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 proper steam circulation and compromise the sterility of the contents.

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

The maintenance of this dental sterilization container primarily relies on the regular inspection of the Teflon filters and the sealing gaskets. Although the 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 neutral pH solutions to avoid oxidation of the walls or degradation of the components. It is recommended to scrupulously follow the autoclave drying cycles to prevent 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 location is essential.

Who is the manufacturer and which standards are met?

This product is manufactured according to rigorous quality standards to meet the requirements of healthcare professionals. Although specific certifications (such as 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.