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Double Surgical Excavator Helmut Zepf for Dental Surgery

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The Excavateur chirurgical double Helmut Zepf pour is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • 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 double surgical excavator?

The Helmut Zepf double surgical excavator is a precision manual instrument designed for oral surgery procedures and conservative care. Manufactured from medical stainless steel by Helmut Zepf Medizintechnik GmbH, this instrument is characterized by a double active-ended structure. Its design allows practitioners to effectively access different areas of the oral cavity for tissue removal. As a Class I device, it meets quality requirements for repeated use after a complete reprocessing cycle. The steel used provides the necessary rigidity for curettage movements while ensuring standard biocompatibility for non-invasive or transient devices.

What are the clinical indications?

This surgical excavator is primarily indicated as a manual dental instrument for the removal of carious dentin and the cleaning of cavities before filling. In surgery, it is used for alveolar curettage, the removal of granulation tissue, or debris during extractions or apical resections. Its use is strictly reserved for healthcare professionals trained in dental and oral surgery techniques. The instrument allows for a precise tactile approach, essential for distinguishing healthy tissue from pathological tissue during the preparation of surgical sites or restorative cavities.

What are the technical characteristics?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH in medical-grade stainless steel, offering corrosion resistance and durability suitable for sterilization cycles. It is a double instrument, featuring two active parts allowing for alternating angles of attack without changing tools. The manufacturer delivers these products non-sterile, requiring complete processing before the first use. The instrument's design does not define a maximum limit of treatment cycles, as this depends on visible wear, the potential presence of cracks, or defects on the cutting edges which must be systematically checked by the practitioner.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or metal intolerance. If a hypersensitivity reaction is triggered in the patient upon contact with the medical stainless steel, the procedure must be stopped immediately. Necessary medical measures must then be taken accordingly. It is therefore crucial to question the patient about their history of allergies to metallic components before any intervention. Furthermore, the use of the instrument is contraindicated if it shows visible damage such as breaks or blunt edges, as this could compromise the safety of the treatment or the integrity of the tissues.

What are the maintenance and sterilization precautions?

All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is imperative to perform a complete cleaning to remove any residue before the sterilization cycle. The practitioner must inspect the excavator to detect any signs of wear, corrosion, or deformation. The use of damaged products is strictly prohibited. Given that the devices are delivered non-sterile, compliance with current reprocessing protocols in dental offices or hospital environments is mandatory to ensure the asepsis and longevity of the stainless steel instrument.

Who is the manufacturer and what standards are respected?

The official manufacturer is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer specifies that compatibility with other products used during the intervention must be verified beforehand. As a Class Ir instrument (according to technical marking MDC0483), it follows rigorous manufacturing processes in accordance with European standards for manual instruments. Traceability and compliance with safety requirements are ensured by Helmut Zepf, a recognized player in the field of dental surgical instrumentation.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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