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Heidbrink. Fragment Decorticator - Helmut Zepf (17.052.03) - Delynov

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The Heidbrink. Décortiqueur à Fragments - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 17.052.03.
  • Reserved for healthcare professionals. Read instructions carefully before use.

64.37 € 64.37 EUR 64.37 € Tax Included

64.37 € Tax Included

(64.37 € / Units)
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Instrument

What is the Helmut Zepf Heidbrink?

The Heidbrink (reference 17.052.03) is a fragment ejector designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This manual instrument belongs to the category of dental surgery consumables and instruments. It is manufactured from medical stainless steel, a standard material for surgical instrumentation ensuring resistance to cleaning and sterilization processes. This device is specifically structured for the fine manipulation of small fragments within the oral cavity. As a Class I device, it meets the basic regulatory requirements for non-invasive or short-term invasive instruments used in clinical practice by qualified healthcare professionals.

What are the clinical indications for this instrument?

The Helmut Zepf Heidbrink instrument is indicated for use as a manual dental instrument during various oral and implant surgery procedures. Its primary use lies in the decortication and extraction of fragments, whether they are root residues after a complex extraction or small bone chips generated during an osteotomy. It is particularly useful for cleaning alveolar sites and ensuring the removal of any foreign bodies or tissue debris before flap closure or the placement of filling material. Its design allows access to restricted areas to secure the operative field.

What are the technical characteristics of the 17.052.03 ejector?

The Heidbrink fragment ejector, bearing technical reference 17.052.03, is a manual instrument developed by Helmut Zepf. It is designed from high-quality medical stainless steel to ensure durability during reprocessing cycles. This device is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use as well as between each patient. Its design is optimized for grip and precise manipulation of small elements. As a Class I device, it is subject to rigorous quality controls by the manufacturer Helmut Zepf Medizintechnik GmbH, guaranteeing its compliance with professional dental instrumentation standards.

What are the contraindications for the use of this instrument?

The main documented medical contraindication for this Helmut Zepf instrument concerns hypersensitivity or known intolerance to metals. Since the device is manufactured from medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. The manufacturer specifies that a hypersensitivity reaction can always occur; in such a case, the surgical procedure must be immediately stopped and necessary medical measures must be taken. It is therefore imperative to check the patient's history regarding allergies to metallic components (such as nickel or chromium) before any intervention with this manual instrument.

What are the maintenance and reprocessing precautions?

The Heidbrink ejector is a reusable instrument that requires strict maintenance. Before the first use and after each surgical act, the instrument must be cleaned, disinfected, and sterilized according to current protocols. The practitioner must imperatively inspect the product before use to detect any visible damage such as cracks, breaks, or defects on the active parts. It is strictly forbidden to use a damaged or worn product. Due to its design and the materials used, Helmut Zepf indicates that there is no defined maximum limit of treatment cycles, but compatibility with other cleaning products must be verified beforehand by the professional.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This fragment ejector is classified as a Class I medical device according to current regulations. The manufacturer follows strict manufacturing protocols to guarantee the safety and efficacy of its manual instruments. The mention of Class Ir and associated references (MDC0483) underlines the manufacturer's commitment to European regulatory compliance. This product is exclusively reserved for use by trained healthcare professionals, thus ensuring an application compliant with clinical standards of dental and oral surgery.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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