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Retrograde Instrument - Helmut Zepf (24.725.70) - Delynov

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The Instrument rétrograde - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.725.70.
  • Reserved for healthcare professionals. Read instructions carefully before use.

66.72 € 66.72 EUR 66.72 € Tax Included

66.72 € Tax Included

(66.72 € / Units)
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Instrument

What is the Helmut Zepf (24.725.70) retrograde instrument?

The retrograde instrument referenced 24.725.70 by Helmut Zepf is a manual device designed for endodontic micro-surgery. Manufactured from medical stainless steel, this micro-endo instrument features a structure adapted to the requirements of apical surgery. It belongs to the category of precision manual instruments developed by Helmut Zepf Medizintechnik GmbH to meet the needs of practitioners specializing in surgical endodontics. Its metallic composition ensures the necessary rigidity while respecting biocompatibility standards for temporary contact with oral tissues, provided there is no known patient hypersensitivity to the steel components.

What are the clinical indications for this instrument?

This retrograde endo instrument is primarily indicated for apical resection and a retro filling interventions. Within the framework of endodontic surgery, it allows for the manipulation of filling materials or the cleaning of the prepared cavity at the root tip. Its use is reserved for qualified healthcare professionals practicing oral surgery and endodontics. It is particularly useful when orthograde access is impossible or has failed, requiring a direct surgical approach to the apex. The instrument must be used exclusively for its intended purpose of manual dental manipulation.

What are the technical characteristics of this device?

The Helmut Zepf (24.725.70) instrument is characterized by its high-quality medical stainless steel manufacture. Classified as a Class I medical device (Classe Ir according to the reference text), it is delivered non-sterile by the manufacturer Helmut Zepf Medizintechnik GmbH. Its technical design is optimized for durability and resistance to repeated reprocessing cycles, although no maximum cycle limit is defined by the manufacturer due to the nature of the materials. It must imperatively undergo complete cleaning, disinfection, and sterilization before the first use and after each subsequent use.

What are the contraindications for the use of this instrument?

The main documented medical contraindication is hypersensitivity or intolerance to metals. As the instrument consists of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. Furthermore, it is formally advised not to use the instrument if it shows visible damage, such as cracks, breaks, or defects on the active parts, to ensure patient safety and the effectiveness of the surgical act.

What are the maintenance and sterilization precautions?

As Helmut Zepf products are delivered non-sterile, a strict reprocessing protocol is mandatory. Before the first use, and between each patient, the instrument must be cleaned, disinfected, and sterilized. The practitioner must visually inspect each product for wear or damage before use. It is crucial to check compatibility with other instruments used simultaneously. Due to its robust stainless steel design, there is no predefined cycle limit, but the physical condition of the instrument (absence of cracks or edge defects) determines its operational end-of-life. The use of damaged or worn products is strictly prohibited.

Who is the manufacturer and what standards are met?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This device is a Class I instrument, compliant with regulatory requirements for manual medical devices. Manufacturing follows medical stainless steel quality standards to ensure clinical safety. As a Classe Ir device (according to the mentioned marking), it meets the cleaning and sterilization protocols defined by the manufacturer for reusable instruments. Compliance with the safety and usage instructions provided by Helmut Zepf is imperative to maintain conformity and safety during surgical procedures.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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