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LUCAS. CURETTE. FIG.2 - Helmut Zepf

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The Curette Lucas Fig.2 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 41.855.02Z.
  • Reserved for healthcare professionals. Read instructions carefully before use.

71.04 € 71.04 EUR 71.04 € Tax Included 144.22 €

71.04 € Tax Included 144.22 €

(0.00 € / Units)
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Instrument

What is the Helmut Zepf Lucas Fig.2 curette?

The Lucas Fig.2 curette, referenced under code 41.855.02Z by the manufacturer Helmut Zepf Medizintechnik GmbH, is a high-precision manual dental instrument. Designed in medical stainless steel, this double-ended curette is structured to meet the requirements of dental surgeons during operative phases. Its robust design allows for reliable handling for cleaning sockets or tissue excision. As a Class I device, it meets basic safety standards for non-invasive or surgically invasive instruments for temporary use, ensuring manufacturing quality consistent with the expectations of healthcare professionals.

What are the clinical indications for this instrument?

The intended use of the Helmut Zepf Lucas Fig.2 curette primarily concerns surgical treatments involving the tooth or dental apparatus. It is indicated for the removal of granulation tissue, cleaning sockets after tooth extraction, or during apical surgeries. This instrument is essential for ensuring mechanical decontamination of infected sites before potential implant placement or bone regeneration. Its application is strictly reserved for qualified healthcare professionals mastering oral surgery and implantology protocols, in order to guarantee a precise and safe clinical procedure for the patient.

What are the technical characteristics of the 41.855.02Z curette?

The Lucas Fig.2 curette (reference 41.855.02Z) is distinguished by its manufacture in medical stainless steel, a material chosen by Helmut Zepf for its corrosion resistance and durability. It is a non-sterile manual instrument with a double active end, allowing for versatility of movement during curettage. Its geometry is specifically adapted to access difficult alveolar areas. Before any use, the practitioner must imperatively check for the absence of visible damage, such as cracks, breaks, or defects on the cutting edges, as the use of worn or damaged products is prohibited to maintain the effectiveness of the surgical procedure.

What are the contraindications for the use of this instrument?

The main documented medical contraindication for this Helmut Zepf instrument is hypersensitivity or intolerance to metals. Since the curette is manufactured from medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If such a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and the necessary clinical measures must be taken. It is the practitioner's responsibility to evaluate the patient's allergic history before any surgical handling with metallic instruments to prevent any undesirable side effects related to the materials.

What are the maintenance and sterilization precautions?

Helmut Zepf Medizintechnik GmbH products are delivered non-sterile. It is mandatory to clean, disinfect, and sterilize the instrument before the first use, as well as before each subsequent use. The full reprocessing cycle must be scrupulously followed to guarantee asepsis. Due to the quality of the materials used and the design of the Lucas Fig.2 curette, there is no defined maximum limit of treatment cycles, as long as the instrument does not show signs of wear or functional degradation. The practitioner must also verify compatibility with other products and devices used during the sterilization chain.

Who is the manufacturer and what standards are respected?

The Lucas Fig.2 curette is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer ensures the traceability and compliance of its instruments with safety requirements for professional use in dental offices or hospital environments. Compliance with the cleaning and sterilization protocols described by the manufacturer is essential to maintain product conformity. This device is exclusively reserved for healthcare professionals trained in dental and oral surgery techniques.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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