Sterilization Container - Helmut Zepf (85.327.00) - Delynov

What is the Helmut Zepf sterilization container (85.327.00)?

The Helmut Zepf sterilization container, referenced under code 85.327.00, is a Class I medical device designed for the rigorous management of instrumentation in surgical environments. Manufactured by Helmut Zepf Medizintechnik GmbH, this product is an aluminum sterilization box or technical housing intended to hold manual dental instruments before their processing cycle. Its structure is specifically designed to withstand repeated cleaning, disinfection, and sterilization processes, thus guaranteeing optimal organization of the technical platform within the practice.

What are the clinical indications for this device?

This dental instrument container is indicated for the storage and reprocessing of manual instruments used during dental surgery, implantology, or periodontology procedures. Its primary use is to serve as logistical support during all stages of the sterilization chain. It allows instruments to be grouped by surgical protocol, ensuring immediate and secure availability of equipment for the practitioner. As a surgery sterilization system, it actively participates in maintaining hygiene and preventing cross-contamination in clinical settings.

What are the technical characteristics of this container?

The Helmut Zepf container (85.327.00) is developed from resistant materials adapted to the thermal and chemical constraints of autoclaves. Although delivered non-sterile, it is designed to undergo unlimited processing cycles, as no maximum limit is defined by the manufacturer due to the robustness of the materials used. Its design allows for optimal circulation of sterilizing agents. It is imperative to check for the absence of visible damage, such as cracks or deformations, before each use to guarantee the effectiveness of the sterilization process.

What are the contraindications for the use of this equipment?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns metal intolerance. Although the container is a sterilization accessory, direct or indirect contact with medical stainless steel instrumentation can trigger hypersensitivity reactions in certain patients. If such a reaction occurs during the clinical procedure, the intervention must be immediately interrupted and necessary medical measures must be taken. It is therefore crucial to evaluate the patient's allergic history before any manipulation of instruments stored in these devices.

What are the maintenance and safety precautions?

All products delivered by Helmut Zepf Medizintechnik GmbH must imperatively be cleaned, disinfected, and sterilized before their first use, as well as before each subsequent use. The practitioner must perform a meticulous visual inspection to detect any wear, cracks, or defects on the edges. The use of damaged products is strictly prohibited. Compatibility with other cleaning devices must also be verified beforehand. This equipment is exclusively reserved for healthcare professionals trained in medical device reprocessing protocols.

Who is the manufacturer and what standards are respected?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This product belongs to Class I according to current medical device regulations (MDR). As a recognized manufacturer in the dental instrumentation sector, Helmut Zepf guarantees a manufacturing process compliant with safety and performance requirements. Compliance with cleaning and sterilization instructions is essential to maintain device conformity and ensure the safety of care during each surgical intervention.

State of the art

Surgical medical consumables play a decisive role in operative safety.