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130 Length Pressor - Helmut Zepf (85.182.04) - Delynov

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The Presseur de longueur 130 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 85.182.04.
  • Reserved for healthcare professionals. Read instructions carefully before use.

35.10 € 35.1 EUR 35.10 € Tax Included

35.10 € Tax Included

(35.10 € / Units)
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Instrument

What is the Helmut Zepf length 130 compactor?

The length 130 compactor, referenced under code 85.182.04, is a manual instrument designed by Helmut Zepf Medizintechnik GmbH. This bone compaction instrument is manufactured from medical stainless steel, ensuring resistance adapted to the constraints of oral surgery. Its structure is specifically designed to offer a direct grip during the condensation phases of graft materials. As a Class I device, it meets the basic safety requirements for non-invasive or short-term invasive instruments. Its simple and robust design makes it a standard tool for handling bone substitutes in dental practices.

What are the clinical indications for this dental surgery compactor?

This dental surgery compactor is indicated for all procedures requiring effective bone compaction. In implantology, it is used to condense autogenous, allogeneic, or synthetic bone particles within a bone defect or an extraction socket. It is particularly useful during sinus lifts or ridge augmentations, where the density of the filling material must be optimized to promote neo-angiogenesis and the future stability of the implant. The instrument allows for the application of precise axial pressure to eliminate void spaces within the graft, thus ensuring better biological integration of the substitute used.

What are the technical characteristics of this surgical compression instrument?

The Helmut Zepf compactor (reference 85.182.04) has a total length of 130mm, giving it optimal maneuverability in restricted access areas of the oral cavity. Manufactured by Helmut Zepf Medizintechnik GmbH, this surgical compression instrument is delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and after each procedure. Its medical stainless steel composition ensures durability against repeated thermal reprocessing cycles. Its geometry is designed to transmit the operator's force homogeneously to the working tip, thus avoiding the dispersion of the filling material during the compaction movement.

What are the contraindications for the use of this instrument?

According to data from the manufacturer Helmut Zepf, the main medical contraindication lies in the patient's known hypersensitivity or intolerance to metals, and more particularly to the components of medical stainless steel. If a hypersensitivity reaction occurs during the procedure, the procedure must be immediately interrupted and the necessary clinical measures must be taken. Furthermore, the use of the instrument is strictly reserved for qualified healthcare professionals. The use of an instrument showing visible damage, such as cracks, breaks, or surface defects, is formally prohibited to avoid any risk of intraoperative rupture or cross-contamination.

What are the maintenance and reprocessing precautions?

As the compactor is a non-resorbable and reusable instrument, it requires a rigorous reprocessing protocol. Before each use, the practitioner must check for the absence of wear or structural damage. Cleaning must be complete to eliminate all organic residue before the sterilization phase. Due to its robust stainless steel design, the manufacturer does not establish a defined maximum limit for treatment cycles, as long as the functional and visual integrity of the instrument is preserved. It is crucial to check compatibility with other products and cleaning agents used to prevent any premature corrosion of the steel.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Germany. This compactor is classified as a Class I medical device according to current regulations. The manufacturer specifies that all products must be cleaned, disinfected, and sterilized before any use, as they are delivered non-sterile. Compliance with reprocessing protocols (MDC0483) is essential to guarantee the safety of the patient and the practitioner. As a manual dental instrument, it is intended exclusively for professional use in a clinical environment, respecting the manufacturing standards of the Helmut Zepf brand for stainless steel surgical devices.


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Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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