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Surgical drill for bone drilling, diameter 2.0mm, depth 12mm - Helmut Zepf (08.524.19) - Delynov

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The Fraise chirurgicale pour perçage osseux, diamètre 2,0 mm, profondeur 12 mm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 08.524.19.
  • Reserved for healthcare professionals. Read instructions carefully before use.

44.08 € 44.08 EUR 44.08 € Tax Included

44.08 € Tax Included

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Instrument

What is the Helmut Zepf 08.524.19 surgical bur?

The surgical bone drilling bur referenced 08.524.19 is a precision rotary instrument designed by Helmut Zepf Medizintechnik GmbH. This device is specifically developed for oral surgery interventions requiring controlled alteration of hard tissues. Its structure is optimized for bone drilling with fixed dimensions, guaranteeing repeatability of the surgical gesture. As part of the dental office consumables category, it meets the performance requirements expected by implantologists and oral surgeons during bone site preparation.

What are the clinical indications for this dental bone bur?

This dental bone bur is indicated for all procedures requiring precise drilling in cortical or cancellous bone. It is mainly used in implant surgery for recipient site preparation, but also in general oral surgery for creating anchor points or passing bone suture wires. Its use is common during osteotomy protocols or bone harvesting where a drilling diameter of 2.0 mm is required. It allows for efficient bone drilling while respecting standard irrigation protocols to limit thermal heating of surrounding tissues.

What are the technical characteristics of the 08.524.19 bur?

The Helmut Zepf bone drilling bur features strict technical characteristics to meet the needs of modern implantology. It has a cutting diameter of 2.0 mm, which corresponds to initial or intermediate drilling standards in many systems. The working depth is fixed at 12 mm, allowing for visual and physical control of penetration into the bone tissue. Reference code 08.524.19 precisely identifies this model within the manufacturer Helmut Zepf Medizintechnik GmbH catalog, ensuring traceability and compatibility with standard surgical handpieces used in the office.

What are the contraindications for the use of this bone drilling bur?

Contraindications for the use of this bone drilling bur are mainly related to the patient's clinical conditions and the technical limits of the instrument. Its use is prohibited in cases of insufficient bone density that does not allow for stable guidance of the bur, or conversely, on non-biological materials for which it is not designed. As with any surgical rotary instrument, the absence of adequate external irrigation constitutes a major contraindication to avoid thermal necrosis. Known allergies to the metallic components of the instrument should also be verified before any intervention.

What are the precautions for use and maintenance for this device?

The use of the dental bone drilling bur requires an adapted rotation speed and moderate pressure to preserve tissue integrity and the longevity of the cutting edge. Although specific resorption data do not apply to this non-implantable tool, post-operative precautions concern the management of the drilled site. The instrument must be inspected before each use to detect any signs of wear or deformation. Compliance with the cleaning, disinfection, and sterilization cycles recommended by the manufacturer Helmut Zepf is imperative to guarantee patient safety and the maintenance of the bur's cutting capabilities.

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-quality surgical instrumentation. Although the regulatory class and specific CE marking are not detailed in the current technical sheet, the product is designed according to the rigorous manufacturing standards of the German medical industry. Practitioners are invited to systematically refer to the instructions for use and labeling provided with the product to verify current certifications, validated sterilization protocols, and compliance with European Medical Device Regulations (MDR).


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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