Autoclavable 134°C 0.2 µm Filters (DEMICAP) - EDRA Medical - Delynov

What is the 134°C 0.2 µm autoclavable filter (DEMICAP)?

The 134°C 0.2 µm autoclavable filter, bearing the technical reference DEMICAP from the brand EDRA MEDICAL, is a high-performance filtration device intended for clinical environments. This sterilization filter is specifically designed to retain particles and micro-organisms down to a threshold of 0.2 micron. Its robust structure allows it to withstand repeated sterilization cycles in an autoclave at a temperature of 134°C, thus guaranteeing durability and reliability essential for maintaining asepsis. Offered in a pack of three units by EDRA Médical and distributed by Delynov, this consumable is a key element for the protection of air circuits and the management of sterile flows during the preparation of surgical equipment.

What are the clinical indications for this 0 2 micron medical filter?

In oral, implant, and periodontal surgery, maintaining a flawless sterilization chain is imperative. The 0 2 micron medical filter from the brand EDRA MEDICAL is indicated for the filtration of air and fluids within sterilization systems. It is used to prevent any cross-contamination by blocking the passage of pathogens during vacuum phases or pressure balancing in the medical pressure cooker. This device is particularly suitable for practices performing invasive procedures where the purity of the sterilization environment directly impacts the post-operative safety of patients. Its regular use helps secure the processing of ancillaries and rotary instruments.

What are the technical characteristics of the DEMICAP filter?

The DEMICAP sterilization filter presents precise technical specifications to meet the thermal and physical constraints of saturated steam sterilization. Its main characteristic is its 0.2 µm porosity, a standard for sterilizing air filtration. It is designed to withstand a temperature of 134°C, corresponding to the most common Class B cycles in dental practices. The manufacturer's design emphasizes air permeability while ensuring maximum bacterial retention. This set of three filters allows for efficient equipment rotation, ensuring that the practitioner always has an operational filter for their daily decontamination cycles.

What are the contraindications for the use of this autoclave air filter?

The use of the autoclave air filter from the brand EDRA MEDICAL does not present direct medical contraindications for the patient, as it does not come into contact with human tissue. However, its use is contraindicated outside the technical parameters specified by the manufacturer. It must not be exposed to temperatures exceeding 134°C or to incompatible sterilization processes (such as dry heat or certain aggressive chemical agents) that could alter the 0.2 µm membrane. Furthermore, the use of a damaged, clogged filter or one that has exceeded the recommended number of cycles is strongly discouraged, as this would compromise the effectiveness of the filtration barrier and the final sterility of the devices.

What are the maintenance and replacement precautions for the filter?

Although this filter is autoclavable, strict precautions should be followed to guarantee its longevity. After each cycle at 134°C, a visual inspection is recommended to detect any deformation or degradation of the DEMICAP structure. Replacement must be carried out systematically according to the manufacturer's recommendations or if abnormal resistance to airflow is noted, a sign of clogging of the 0.2 micron membrane. A saturated filter can harm autoclave performance and compromise instrument drying. It is advisable to keep a cycle tracking log for each filter to ensure regular renewal in accordance with the practice's hygiene protocols.

Who is the manufacturer and what standards are met?

This product is manufactured by the manufacturer and distributed under the brand EDRA MEDICAL by EDRA Médical via the Delynov platform. As a Class CONSO consumable, it is designed to meet the technical requirements for filtration in a medical environment. Although specific certifications (regulatory class or precise CE marking) are not detailed in the source documentation, the device is developed to satisfy the 0.2 µm filtration standards required for steam sterilization. Professionals are invited to scrupulously refer to the instructions for use and technical data sheets provided by the manufacturer to validate the filter's compliance with their specific autoclave model and internal sterility validation protocols.

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