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Roots - Helmut Zepf (12.045.15Z) - Delynov

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The Racines - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 12.045.15Z.
  • Reserved for healthcare professionals. Read instructions carefully before use.

146.59 € 146.59 EUR 146.59 € Tax Included 287.26 €

146.59 € Tax Included 287.26 €

(0.00 € / Units)
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Instrument

What is the Helmut Zepf 12.045.15Z root forceps?

The Helmut Zepf root forceps, referenced under code 12.045.15Z, is a high-precision surgical instrument manufactured from medical stainless steel. This device, belonging to the consumables category (CONSO), is specifically designed for extraction procedures in oral surgery. Its robust structure allows for reliable handling when grasping radicular fragments or implants. As a Helmut Zepf Medizintechnik GmbH product, it benefits from the expertise of a manufacturer recognized for the quality of its stainless steel instruments, guaranteeing resistance adapted to the mechanical stresses of exodontia and explantation procedures.

What are the clinical indications for this universal root forceps?

This universal root forceps is indicated for two major clinical applications in dental practices and hospital environments. Firstly, it serves as root forceps for the extraction of natural dental roots or persistent radicular remains after a crown fracture. Secondly, it is used as explantation forceps for the removal of artificial dental roots, commonly known as dental implants. Its use is strictly reserved for qualified healthcare professionals involved in oral surgery, implantology, or periodontology protocols requiring the removal of structures deeply anchored in the alveolar bone.

What are the technical characteristics of the 12.045.15Z device?

The Helmut Zepf 12.045.15Z instrument is characterized by its manufacture in high-quality medical stainless steel. Classified as a Class I medical device, it meets the safety requirements for non-invasive or invasive instruments for temporary use. The product is delivered non-sterile, which necessitates a rigorous cleaning, disinfection, and sterilization protocol before the first use and between each patient. Due to its design and the materials used, the manufacturer Helmut Zepf does not define a maximum limit for processing cycles, although the user must inspect the instrument for any cracks, breaks, or defects on the edges before each procedure.

What are the contraindications for using this instrument?

The main medical contraindication related to the use of these forceps lies in the patient's known hypersensitivity to metals. Contact with medical stainless steel can trigger allergic or intolerance reactions in certain individuals. If a hypersensitivity reaction is observed during the procedure, the process must be immediately stopped and the necessary clinical measures must be taken. It is therefore imperative to check the patient's allergic history before any manipulation. Furthermore, the use of the instrument is contraindicated if it shows visible damage, such as cracks or excessive wear on the active parts.

What are the maintenance and reprocessing precautions?

Reprocessing of the Helmut Zepf forceps must follow strict steps: cleaning, disinfection, and complete sterilization. Before the first use, the instrument must mandatory be treated. The practitioner must check compatibility with other cleaning products and ensure that no visible damage impairs the safety of the device. Although the number of sterilization cycles is not limited by a fixed value, the longevity of the tool depends on compliance with maintenance protocols. The use of damaged or worn products is formally prohibited to guarantee tissue integrity during the extraction of roots or implants.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, headquartered in Seitingen-Oberflacht, Germany. This manufacturer is globally recognized for its dental surgery instruments. The product complies with the Class I medical device regulations. Safety instructions stipulate that all instruments must be inspected for any cracks or breakage before use. Traceability is ensured by the technical reference 12.045.15Z. Helmut Zepf emphasizes that its products are exclusively reserved for healthcare professionals, guaranteeing use in accordance with current clinical standards in exodontia and implant surgery.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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