Angled Shape of Fig.35A - Helmut Zepf (12.035.01Z)

What is the Angular Shape Fig.35A - Helmut Zepf?

The Angular Shape Fig.35A, referenced under code 12.035.01Z, is a surgical instrument manufactured by Helmut Zepf Medizintechnik GmbH. It is a device similar to dental forceps, specifically designed for tooth extraction. This instrument is crafted from medical stainless steel, a standard material for surgical instrumentation ensuring the necessary robustness during avulsion procedures. As a Class I device, it meets the regulatory requirements for non-invasive or invasive instruments for temporary use used in dental offices and hospital settings.

What are the clinical indications?

This Helmut Zepf instrument is exclusively indicated for tooth extraction. Its use occurs within the framework of oral and alveolar surgery, when the practitioner must proceed with the exodontia of a dental element. The angular configuration of the Fig.35A allows for manipulation adapted to the anatomical constraints of the oral cavity. The use of this device is strictly reserved for qualified healthcare professionals, mastering extraction techniques and associated surgical protocols to ensure optimal patient care during dental removal procedures.

What are the technical characteristics of this instrument?

The Helmut Zepf 12.035.01Z instrument is characterized by its manufacture from high-quality medical stainless steel. Its Fig.35A design features a specific angular geometry to facilitate access and the transmission of forces during extraction. The manufacturer specifies that, due to the product design and the materials used, there is no defined maximum limit for achievable processing cycles, although wear must be monitored. The products are delivered non-sterile and must imperatively undergo a complete preparation cycle before each use.

What are the contraindications for use?

The main contraindication related to the use of this instrument is hypersensitivity or intolerance to metals. Contact with medical stainless steel can trigger a hypersensitivity reaction in certain sensitive patients. If such a reaction occurs during the procedure, the manufacturer Helmut Zepf stipulates that the intervention must be immediately stopped and necessary medical measures must be taken. It is therefore crucial to check the patient's allergic history before any manipulation of the instrument in the mouth to prevent these undesirable side effects.

What are the maintenance and safety precautions?

Before the first use and after each subsequent use, the instrument must be fully cleaned, disinfected, and sterilized. The manufacturer insists on the importance of checking the condition of the steel before each intervention: it is imperative to look for visible damage such as cracks, breaks, or defects on the cutting edges. Any instrument showing signs of wear or structural damage must never be used. Compatibility with other products used simultaneously must also be verified beforehand to ensure the safety of the surgical field and the effectiveness of the surgical gesture.

Who is the manufacturer and what standards are respected?

This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer respects the safety and traceability protocols imposed by health authorities for dental instrumentation. The instructions provided emphasize that reprocessing is possible thanks to the quality of the materials, without a predefined cycle limit, subject to a rigorous inspection of the physical integrity of the instrument. This equipment is exclusively intended for use by trained healthcare professionals.

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