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Angular Shape Figurine 36 - Helmut Zepf (12.036.00Z) - Delynov

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The Forme Angulaire de la Figurine 36 - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 12.036.00Z.
  • 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 12.036.00Z forceps?

The Figurine 36 angular forceps, referenced under code 12.036.00Z, is a manual instrument designed by Helmut Zepf Medizintechnik GmbH. This medical device is manufactured from high-quality medical stainless steel, a standard material for surgical instrumentation ensuring the structural resistance necessary for the forces exerted during extractions. Its angular configuration is specifically studied to meet the ergonomic and technical needs of dental surgeons during avulsion procedures. As a Class I device, it meets the basic regulatory requirements for non-invasive or short-term invasive instruments used in clinical dental practice.

What are the clinical indications for this instrument?

According to the specifications of the manufacturer Helmut Zepf, this instrument is exclusively indicated for the extraction of teeth. Its use is reserved for health professionals qualified in oral and dental surgery. The angular shape of the Figurine 36 allows for approaching certain areas of the dental arch where straight forceps might be less suitable. It is used to grasp the tooth at the neck or root level to apply the luxation and traction forces necessary for alveolar avulsion. Its application is part of simple or complex extraction protocols prior to eventual prosthetic or implant rehabilitation.

What are the technical characteristics of the 12.036.00Z forceps?

The Helmut Zepf 12.036.00Z forceps is characterized by its medical stainless steel construction, offering durability compatible with repeated reprocessing cycles. It is a Class I instrument, delivered non-sterile, which requires a strict preparation protocol before any use. The design of the instrument does not define a maximum limit for treatment cycles, as this depends on maintenance and the eventual appearance of visible damage. The practitioner must imperatively inspect the instrument before each use to detect cracks, breaks, or defects on the active parts, thereby ensuring operational safety.

What are the contraindications for the use of this instrument?

The main medical contraindication documented by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known patient hypersensitivity to metals. As the instrument is composed of medical stainless steel, contact may trigger an intolerance or hypersensitivity reaction in certain subjects. If such a reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore crucial to check the patient's anamnesis regarding metal allergies before any use of this surgical instrument in the mouth.

What are the maintenance and sterilization precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. Cleaning must be complete to eliminate all biological residue. Before sterilization, a visual inspection is necessary to identify any wear, cracks, or corrosion. The use of damaged products or those presenting defects on the cutting edges is strictly prohibited. Due to the quality of the materials used, there is no fixed limit to the number of sterilization cycles, but the longevity of the forceps depends directly on compliance with the cleaning and disinfection instructions recommended by the manufacturer.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to the current regulations. The products are delivered non-sterile and must be processed by the healthcare professional in accordance with hospital or office sterilization protocols. The manufacturer emphasizes that the use of these instruments is strictly reserved for healthcare professionals. Compliance with medical stainless steel standards ensures that the instrument can undergo the disinfection and sterilization processes required for patient safety in dental surgery.


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Specifications

Manufacturer Helmut Zepf
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