AMERICAN FORM FIGURE 17 - Helmut Zepf (14.017.00) - Delynov

What is the Helmut Zepf American pattern figure 17 extraction forceps?

The American pattern figure 17 extraction forceps, referenced under code 14.017.00 by Helmut Zepf, is a manual instrument specifically designed for exodontia. Manufactured from high-quality medical stainless steel, this device is intended for the grasping and extraction of molars from the mandibular arch. Its robust structure meets the requirements of oral surgery interventions, offering the necessary resistance to the torsion and traction forces applied during complex dental extractions.

What are the clinical indications for this instrument?

The primary indication for this manual dental instrument is the extraction of lower molars. In clinical practice, it is used by dental surgeons and implantologists during oral surgery procedures to remove teeth condemned by advanced caries, periodontal disease, or as part of pre-implant treatment plans. Its American pattern figure 17 is optimized to adapt to the coronal morphology of mandibular molars, allowing for effective force transmission during luxation.

What are the technical characteristics of the 14.017.00 forceps?

This Helmut Zepf forceps is distinguished by its manufacture in medical stainless steel, a material chosen for its durability and resistance to corrosion. As an American pattern instrument, it features specific ergonomics facilitating access to the posterior areas of the mandible. The product is delivered non-sterile and requires a complete reprocessing cycle before its first use and between each patient. It does not have a defined maximum limit of treatment cycles, as this depends on visible wear and maintenance.

What are the contraindications for the use of this device?

The main medical contraindication is known hypersensitivity or intolerance to metals in the patient, as the instrument is composed of medical stainless steel. If a hypersensitivity reaction is triggered upon contact, the procedure must be immediately stopped and necessary clinical measures must be taken. Furthermore, use is strictly reserved for qualified healthcare professionals proficient in exodontia techniques.

What are the maintenance and safety precautions?

All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is imperative to visually inspect the forceps before each intervention to detect potential damage such as cracks, breaks, or defects on the active parts. The use of damaged or worn products is prohibited to ensure patient safety and the effectiveness of the surgical procedure. The reprocessing process must follow standard hospital sterilization protocols.

Who is the manufacturer and what standards are respected?

The forceps is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer imposes strict cleaning and sterilization instructions to maintain the compliance and safety of the instrument. As a Class I device, it meets the safety and performance requirements for manual dental instruments intended for use by healthcare professionals.

State of the art

Surgical medical consumables play a decisive role in operative safety.