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Sterilization Container Helmut Zepf 310x190x65mm

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The Conteneur de stérilisation Helmut Zepf 310x190x65mm is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reserved for healthcare professionals. Read instructions carefully before use.

254.28 € 254.28 EUR 254.28 € Tax Included

254.28 € Tax Included

(254.28 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf 310x190x65mm sterilization container?

The Helmut Zepf 310x190x65mm sterilization container is a Class I device designed for the packaging and protection of surgical instruments. Manufactured by Helmut Zepf Medizintechnik GmbH, this aluminum sterilization container offers a robust structure adapted to the requirements of dental surgery and implantology practices. Its specific dimensions allow for the efficient organization of technical trays while guaranteeing optimal circulation of sterilization agents. This device is delivered non-sterile and requires complete preparation before its first use within the operating block.

What are the clinical indications for this surgery sterilization box?

This container is indicated for the reprocessing of manual dental instruments used during various clinical interventions. In oral surgery, it serves as a receptacle for the cleaning, disinfection, and final sterilization of tools. The use of this surgery sterilization box is strictly reserved for healthcare professionals trained in asepsis protocols. It maintains the integrity of instruments between interventions, thus avoiding visible damage such as cracks or defects on cutting edges that could compromise the surgical act.

What are the technical characteristics of this device?

This container features dimensions of 310x190x65mm, offering a volume adapted to standard instrument sets. As an aluminum sterilization container, it is designed to withstand repeated treatment cycles without a defined maximum limit, subject to rigorous inspection before each use. The manufacturer Helmut Zepf specifies that the material used allows for thorough cleaning and disinfection. It is imperative to check for the absence of wear, breakage, or deformation on the housing before proceeding with sterilization, as any damaged product must be immediately removed from the clinical circuit.

What are the contraindications for the use of this equipment?

The main contraindication concerns known hypersensitivity to metals. Although the container is used for transport, direct contact with medical stainless steel instruments can cause an intolerance reaction in some patients. If a hypersensitivity reaction is triggered during the procedure, the intervention must be immediately interrupted and the necessary corrective measures must be applied. Furthermore, it is strictly forbidden to use this device if it shows visible damage, cracks, or structural defects compromising the safety of the sterilization process.

What are the maintenance and reprocessing precautions?

All Helmut Zepf products must be fully cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is crucial to perform meticulous cleaning to remove all organic residue before the sterilization cycle. The practitioner must systematically check compatibility with other products used in the cycle. Due to the design and materials, there is no predefined maximum limit of cycles, but longevity depends on scrupulous compliance with safety instructions and the absence of mechanical wear observed during pre-operative inspection.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This product belongs to Class I of medical devices according to current regulations. The manufacturer imposes high quality standards for its manual dental instruments and sterilization accessories. Each aluminum sterilization box must be used in accordance with the instructions provided to ensure the safety of the patient and healthcare staff. Compliance with cleaning and sterilization protocols before any use is an absolute regulatory requirement to maintain the device's conformity in a surgical environment.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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