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Special Bionik Curette - Helmut Zepf (24.207.13GM5OX)

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The ZEPF-BIONIK. CURETTE SPECIALE - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.207.13GM5OX.
  • Reserved for healthcare professionals. Read instructions carefully before use.

88.61 € 88.61 EUR 88.61 € Tax Included

88.61 € Tax Included

(88.61 € / Units)
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Instrument

What is the ZEPF-BIONIK curette?

The ZEPF-BIONIK (reference 24.207.13GM5OX) is a special curette developed by Helmut Zepf Medizintechnik GmbH. It is a manual dental instrument designed for periodontal care. Manufactured from medical-grade stainless steel, its structure is specifically adapted to the requirements of manual instrumentation in oral surgery. This device belongs to Class I of medical devices, ensuring its compliance with regulatory standards for non-invasive or reusable instruments after appropriate processing. Its design aims to meet the needs of practitioners requiring a reliable tool for treating hard and soft tissues of the oral cavity.

What are the clinical indications?

The Helmut Zepf special curette is indicated as a manual dental instrument for various periodontology and prophylaxis procedures. Its primary use concerns the removal of tartar deposits, root planing, and cleaning of periodontal pockets. In oral surgery, it is used for the elimination of granulation tissue or mechanical debridement of surfaces during non-surgical or surgical periodontal treatments. The instrument is exclusively reserved for qualified healthcare professionals, ensuring application in accordance with current clinical protocols for maintaining oral hygiene and the health of supporting tissues.

What are the technical specifications?

This curette, identified under code 24.207.13GM5OX, is manufactured from medical stainless steel by Helmut Zepf. As a Class I instrument, it exhibits resistance suitable for repeated cleaning and sterilization cycles. The manufacturer specifies that, although high-quality materials are used, there is no defined maximum limit for the number of processing cycles achievable; this depends on visible wear and the condition of the cutting edges. Before each use, the practitioner must check for the absence of damage such as cracks, breaks, or defects on the active parts to ensure patient safety and the effectiveness of the surgical procedure.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. Contact with the medical stainless steel of the instrument may trigger an allergic reaction in certain sensitive patients. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore imperative to validate the absence of known allergies to metallic components before any clinical manipulation. Additionally, use of the instrument is prohibited if it shows visible signs of wear or structural damage.

What are the maintenance and sterilization precautions?

Helmut Zepf products are delivered non-sterile and require a strict protocol before any use. All instruments must be cleaned, disinfected, and sterilized before initial use, as well as after each subsequent use. It is crucial to perform a complete cleaning to remove all residues before the sterilization phase. The practitioner must inspect the instrument to detect any trace of corrosion, cracks, or dulling of the sharp edges. The use of damaged or worn products is strictly prohibited. Compatibility with other products used during the procedure must also be verified beforehand to avoid any undesirable interaction.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This device is classified as Class I according to medical device regulations. The manufacturer complies with safety and performance requirements for manual dental instruments. The reprocessing process is left to the discretion of the healthcare professional based on observed wear, as the design and materials used do not allow for an arbitrary definition of a maximum number of sterilization cycles. Traceability is ensured by the technical reference 24.207.13GM5OX, guaranteeing the origin and German manufacturing quality.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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