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ZEPF-BIONIK. CURETTE SPECIALE - Helmut Zepf

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The Curette spéciale Zepf-Bionik - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.207.13G.
  • Reserved for healthcare professionals. Read instructions carefully before use.

63.55 € 63.55 EUR 63.55 € Tax Included

63.55 € Tax Included

(63.55 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf Zepf-Bionik special curette?

The Zepf-Bionik special curette, referenced under code 24.207.13G by Helmut Zepf, is a manual instrument designed for the practice of periodontology and oral surgery. Manufactured from medical stainless steel, this specific dental curette is intended for interventions requiring high technical rigor. It is part of the manual instrument range from the manufacturer Helmut Zepf Medizintechnik GmbH, recognized for the quality of its surgical devices. 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 to ensure the safety of care in the practice.

What are the clinical indications for this instrument?

This manual instrument is primarily indicated for periodontal treatment, including specific scaling and root planing. As a specific dental curette, it provides access to subgingival areas to remove deep calculus and inflammatory tissue. Its use is reserved for healthcare professionals qualified in prophylaxis, periodontology, and implant surgery. It assists in the preparation of root surfaces to promote tissue reattachment. The use of this surgery gracey curette must be preceded by a verification of the instrument's integrity to avoid any risk related to damaged cutting edges.

What are the technical characteristics of the 24.207.13G curette?

The Helmut Zepf curette (reference 24.207.13G) is characterized by its manufacture in high-quality medical stainless steel. Unlike a standard gracey curette, this Zepf-Bionik special model is designed to meet precise ergonomic and clinical needs during curettage phases. It does not include a needle, as it is a rigid manual instrument. Before each intervention, the practitioner must visually inspect the product to detect any cracks, breaks, or defects on the active parts. Due to its design and the materials used, there is no defined maximum limit of processing cycles, as long as the instrument maintains its functional properties and physical integrity.

What are the contraindications for the use of this instrument?

The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Since the instrument is composed of medical stainless steel, contact with the patient can trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the procedure, the use of the instrument must be immediately discontinued and necessary medical measures must be taken. It is therefore crucial to evaluate the patient's allergic history before any intervention. Furthermore, the use of an instrument showing visible damage, such as cracks or excessive wear of the sharp edges, is strictly prohibited.

What are the maintenance and reprocessing precautions?

Helmut Zepf Medizintechnik GmbH products are delivered non-sterile. A complete reprocessing cycle is mandatory before the first use: cleaning, disinfection, and sterilization. This procedure must be repeated after each use. Cleaning must be particularly thorough to remove all biological residues before the sterilization phase. The practitioner must also verify the compatibility of the curette with other cleaning products and devices used in the practice. The absence of a limit on treatment cycles allows for long-term use, provided that maintenance follows the manufacturer's safety instructions and that the wear of the cutting edge does not compromise clinical efficacy.

Who is the manufacturer and what standards are met?

This medical device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. It is a Class I instrument (Class Ir according to nomenclature MDC0483), complying with regulatory requirements for manual medical devices. As a Class I device, it meets the safety and performance standards applicable to reusable surgical instruments. Traceability and manufacturing quality are ensured by the rigorous processes of Helmut Zepf, guaranteeing that each curette meets the needs of dental surgeons and implantologists. The use of this instrument is strictly reserved for healthcare professionals trained in dental surgery techniques.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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