Dental Extraction Forceps (10.685.22) - Delynov - Helmut Zepf - Delynov

What is the English pattern extraction forceps figure 22?

The figure 22 forceps, referenced under code 10.685.22, is a precision manual instrument manufactured by Helmut Zepf Medizintechnik GmbH. It is an English pattern dental extraction forceps, specifically designed for the practice of oral surgery and implantology. This instrument is crafted from high-quality medical stainless steel, ensuring resistance adapted to mechanical stresses during avulsions. As a Class I medical device, it meets regulatory requirements for reusable surgical instruments. Its ergonomic structure allows for optimal force transmission while maintaining a secure grip on the targeted dental structure.

What are the clinical indications for these extraction forceps?

This Helmut Zepf forceps is primarily indicated for the extraction of roots and teeth located in the mandible. In dental surgery, figure 22 is classically used for lower roots. Its use occurs in various clinical contexts such as the avulsion of compromised teeth, site preparation before implant placement, or during guided bone regeneration (GBR) surgeries requiring prior cleaning of the socket. The instrument is strictly reserved for use by qualified healthcare professionals, ensuring handling in accordance with current surgical protocols.

What are the technical characteristics of the 10.685.22 forceps?

The Helmut Zepf figure 22 forceps is distinguished by its English pattern configuration, optimized for access to mandibular areas. Manufactured from medical stainless steel, it is designed to undergo repeated cleaning and sterilization cycles without alteration of its mechanical properties. The manufacturer specifies that due to the robust design and materials used, there is no defined maximum limit for the number of processing cycles, as long as the instrument shows no visible damage. Each product is delivered non-sterile and must undergo complete reprocessing before its first use and between each patient.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. Contact with the medical stainless steel composing the instrument may trigger a reaction in sensitive patients. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to evaluate the patient's allergic history before any surgical handling with this device.

What are the maintenance and safety precautions?

Patient safety and instrument longevity rely on a strict maintenance protocol. All instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is crucial to visually inspect the forceps before each intervention to detect any visible damage or wear, such as cracks, breaks, or defects on the active parts. The use of damaged or worn products is strictly prohibited. Furthermore, compatibility with other products used during surgery must be verified beforehand by the practitioner.

Who is the manufacturer and what standards are respected?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer in the field of surgical instrumentation ensures the compliance of this forceps with European regulatory standards. The product is classified as a Class I medical device (Class Ir according to certain reprocessing nomenclatures). As a precision instrument, it is exclusively intended for healthcare professionals. Compliance with the cleaning and sterilization instructions issued by Helmut Zepf is essential to guarantee microbiological safety and maintain the technical performance of the medical stainless steel used.

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