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Washing basket for bone augmentation kit 47.966.00 - Helmut Zepf (85.194.15) - Delynov

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The Panier de lavage pour kit d'augmentation osseuse 47.966.00 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 85.194.15.
  • Reserved for healthcare professionals. Read instructions carefully before use.

303.38 € 303.38 EUR 303.38 € Tax Included

303.38 € Tax Included

(0.00 € / Units)
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Instrument

What is the washing basket for the Helmut Zepf bone augmentation kit?

The washing basket for bone augmentation kit 47.966.00, referenced under code 85.194.15 by Helmut Zepf, is an instrumental management support specifically designed for oral surgery. This device allows for the grouping of instruments required for graft procedures within a perforated structure. Manufactured by Helmut Zepf Medizintechnik GmbH, this basket facilitates the circulation of cleaning agents and steam. Its design aims to protect delicate instrumentation against mechanical shocks while optimizing the organization of the technical tray in implant or periodontal surgery practices.

What are the clinical indications for this device?

This surgery kit washing basket is indicated for the organization of instruments used during alveolar ridge reconstruction interventions. It is specifically adapted to hold the tools of the Helmut Zepf bone augmentation kit. Its use occurs in the pre-operative phase for sterile field preparation and in the post-operative phase for the processing of reusable medical devices. It finds its application in all bone augmentation surgeries, whether sinus lifts, onlay grafts, or guided bone regeneration, where precise instrument storage is crucial for surgical efficiency.

What are the technical characteristics of the 85.194.15 basket?

The washing basket referenced 85.194.15 features characteristics adapted to modern sterilization protocols. Although exact dimensions are not specified, its structure is optimized to accommodate the complete configuration of the bone augmentation kit 47.966.00. As a kit sterilization cassette, it possesses calibrated perforations to allow total exposure to decontamination solutions and drying cycles. The design by Helmut Zepf Medizintechnik GmbH guarantees compatibility with automated cleaning standards in washer-disinfectors, avoiding shadow zones where biological residues could persist.

What are the contraindications for the use of this basket?

There are no direct clinical contraindications related to the use of this washing basket on the patient, as it is an instrument processing accessory and not an invasive device. However, the use of this bone augmentation washing basket is contraindicated with instruments whose size or shape does not allow for stable maintenance, which could lead to damage during the washing cycle. Additionally, the bone surgery cassette should not be overloaded beyond its intended capacity so as not to compromise the effectiveness of the cleaning and sterilization process.

What are the maintenance and durability precautions?

To guarantee the longevity of this Helmut Zepf device, it is imperative to follow the cleaning protocols validated by the manufacturer. Although the exact material is not listed, this type of surgery sterilization cassette must be inspected regularly to check for the absence of corrosion or deformation of internal fixings. After each washing cycle, complete drying is necessary to avoid any moisture stagnation. The practitioner must ensure that instruments are correctly positioned in their respective slots to avoid any excessive friction that could alter the sharpness or finish of the bone augmentation instruments.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a recognized player in the production of high-precision surgical instrumentation. Regarding specific standards and certifications such as the regulatory class or CE marking, this information is not specified in the current technical documentation. Users are recommended to systematically refer to the instructions for use and the product labeling provided by Helmut Zepf to confirm compliance with the requirements of the European Medical Device Regulation (MDR) and the sterilization protocols in force in their facility.


State of the art

Single-use sterile surgical kits significantly reduce intraoperative contamination.

Specifications

Manufacturer Helmut Zepf
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