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Retrograde Instrument - Helmut Zepf (24.725.73) - 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: 24.725.73.
  • 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 (24.725.73) retrograde instrument?

The Helmut Zepf retrograde instrument, referenced under code 24.725.73, is a manual device designed for endodontic micro-surgery. Manufactured from medical stainless steel by Helmut Zepf Medizintechnik GmbH, this instrument is specifically structured to meet the requirements of apical surgery. As a Class I instrument, it benefits from a rigorous design adapted to clinical environments. Its metallic structure ensures the necessary resistance during delicate manipulations in the root zone. This device is delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and between each patient.

What are the clinical indications for this instrument?

This instrument is primarily indicated for endodontic surgery instrumentation. Its use is recommended during apical surgery procedures, particularly for the retrograde preparation of the apex after an apical resection. It allows the practitioner to access complex areas of the tooth root to ensure the cleaning and shaping of the retrograde cavity before minimal filling. Helmut Zepf apical surgery instrumentation is intended exclusively for healthcare professionals trained in these technical acts, thus guaranteeing an application compliant with current clinical protocols in surgical endodontics.

What are the technical characteristics of reference 24.725.73?

The retrograde instrument referenced 24.725.73 is characterized by its manufacture from high-quality medical stainless steel, selected by Helmut Zepf for its biocompatibility and corrosion resistance. Although specific dimensions are not detailed, its design is optimized for retrograde access. As a Class I device, it meets the safety requirements for reusable manual instruments. The manufacturer specifies that due to the product design and the materials used, there is no defined maximum limit for processing cycles, subject to a visual check for the absence of damage, cracks, or wear on the cutting edges before each use.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. If a patient presents an allergic reaction or intolerance upon contact with the medical stainless steel of the instrument, the procedure must be immediately interrupted. Appropriate medical measures must then be taken. It is therefore crucial to evaluate the patient's allergic history before any intervention. Additionally, the use of the instrument is prohibited if it shows visible defects such as cracks, breaks, or marked wear on the active parts, in order to guarantee patient safety and the effectiveness of the surgical gesture.

What are the maintenance precautions for this non-absorbable instrument?

As a reusable manual instrument and not an absorbable device, maintenance is based on a strict reprocessing protocol. Before the first use and after each procedure, the Helmut Zepf instrument must be cleaned, disinfected, and sterilized. The manufacturer insists on the importance of cleaning each product before checking for any visible damage. It is imperative never to use damaged or worn products, particularly at the level of the cutting edges. Compatibility with other products used during surgery must also be verified beforehand. Compliance with these safety instructions ensures the longevity of the endodontic surgery instrumentation and health safety within the practice.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, headquartered in Seitingen-Oberflacht, Germany. This medical device belongs to Class I (Class Ir according to certain reprocessing nomenclatures). The manufacturer complies with regulatory requirements relating to manual medical devices. Each instrument is delivered non-sterile, leaving the responsibility for reprocessing to the healthcare professional. Following the manufacturer's instructions regarding cleaning and sterilization is mandatory to maintain the compliance of the device. Helmut Zepf is a recognized manufacturer in the dental sector for the quality of its apical surgery instrumentation, guaranteeing high production standards for stainless steel devices.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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