DENTAL EXTRACTION FORCEPS. ENGLISH PATTERN FIGURE 17 - Helmut Zepf (12.017.00Z) - Delynov

What is the Helmut Zepf figure 17 forceps?

The figure 17 forceps, bearing reference 12.017.00Z, is a manual instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This Class I medical device is manufactured from high-quality medical stainless steel. Its structure, known as English form, is specifically adapted to the anatomy of the upper molars. As a non-sterile instrument upon delivery, it requires a complete processing protocol before its first use. Its robust design allows for repeated use in dental surgery practices, subject to rigorous maintenance respecting the manufacturer's instructions.

What are the clinical indications for this forceps?

This upper right molar forceps is indicated for simple or complex exodontia procedures. Its intended purpose is to act as a manual dental instrument for tooth extraction. In clinical practice, it is used by healthcare professionals to firmly grasp the upper right molar in order to apply the rotational and tilting forces necessary to rupture the periodontal ligament. Its use is strictly reserved for qualified practitioners in oral surgery and implantology, thus guaranteeing handling in accordance with current surgical protocols.

What are the technical characteristics of this instrument?

The Helmut Zepf 12.017.00Z forceps is distinguished by its medical stainless steel construction, a material chosen for its mechanical strength and compatibility with sterilization cycles. Although there is no defined maximum limit for processing cycles due to the quality of the materials used, the instrument must undergo systematic visual inspection. The practitioner must check for the absence of visible damage, such as cracks, breaks, or defects on the active parts, before each intervention to ensure patient safety.

What are the contraindications for the use of this device?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity to metal components. A metal intolerance reaction in the patient may result from direct contact with the medical stainless steel of the instrument. If a hypersensitivity reaction is triggered during the surgical procedure, the procedure must be immediately stopped and necessary medical measures must be taken. It is the practitioner's responsibility to check the patient's allergic history before any use of this manual instrument.

What are the maintenance and sterilization precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. The reprocessing process must be complete to ensure asepsis. It is crucial to clean each product individually and check for the absence of wear or damage. The use of damaged products or those showing cracks is strictly prohibited. The manufacturer specifies that the determination of the number of achievable processing cycles depends on the physical condition of the instrument and the rigor of its maintenance.

Who is the manufacturer and what standards are respected?

This forceps is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. The device is classified as Class I according to medical device regulations. The manufacturer imposes strict safety instructions: instruments are delivered non-sterile and their use is exclusively reserved for healthcare professionals. Compliance with cleaning and sterilization protocols, as well as checking compatibility with other products used during the intervention, are essential to maintain the compliance and safety of use of this dental surgery instrument.

State of the art

Surgical medical consumables play a decisive role in operative safety.