EXLOG® DENTAL EXTRACTION FORCEPS FIG. 22 SPECIAL JAWS FOR GRIPPING - Helmut Zepf (15.222.00D) - Delynov

What is the Helmut Zepf EXLOG® Fig. 22 forcep?

The EXLOG® Fig. 22 forcep is an oral surgery instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This specific model, referenced under code 15.222.00D, belongs to the EXLOG® range, characterized by ergonomics and a structure designed to optimize handling during extractions. It is distinguished by the integration of special beaks that allow for precise adaptation to the dental anatomy. This instrument is manufactured according to Helmut Zepf quality standards, guaranteeing durability suitable for intensive clinical use in dental practices or hospital environments for exodontia interventions.

What are the clinical indications for this special beak forcep?

The Fig. 22 special beak extraction forcep is primarily indicated for the extraction of teeth and roots, particularly in the mandible. In oral surgery and implantology, the use of a special beak forcep is crucial when the tooth anatomy or the state of coronal decay requires an optimized contact surface to prevent the instrument from slipping. It is used by practitioners to perform simple or complex avulsions, allowing for effective transmission of the rotational and traction force necessary to rupture the alveolar-dental ligament fibers before the final extraction.

What are the technical characteristics of model 15.222.00D?

The Helmut Zepf model 15.222.00D features technical characteristics specific to the EXLOG® series. Its morphology is of the Fig. 22 type, a recognized standard in dental surgery, but enhanced by special beaks for increased grip. The design of the instrument aims to offer a balance between the fineness of the beaks, allowing subgingival access if necessary, and the robustness of the forcep body to resist mechanical stress. Although exact dimensions are not specified, the Helmut Zepf range is renowned for the precise adjustment of its hinges, limiting functional play and ensuring fluid manipulation during the surgical act.

What are the contraindications for the use of this instrument?

The contraindications for the use of the Helmut Zepf Fig. 22 forcep are mainly related to the limits of conventional exodontia. The use of this instrument is prohibited if the surrounding bone structure or the excessive fragility of the root risks causing a significant unwanted alveolar fracture. As with any surgical steel instrument, it is appropriate to verify the absence of known patient allergy to the alloy components. Furthermore, the use of a forcep unsuitable for the target tooth (for example, using a mandibular forcep for a maxillary tooth) constitutes a technical contraindication that can lead to operative complications or injury to the surrounding soft tissues.

What are the maintenance precautions for this non-resorbable device?

As a reusable steel surgical instrument, the Helmut Zepf forcep requires a rigorous decontamination and sterilization protocol after each use. Practitioners must follow the recommendations of the manufacturer Helmut Zepf Medizintechnik GmbH regarding manual cleaning or washer-disinfector use, as well as standard autoclave cycles. It is imperative to use non-corrosive cleaning agents to preserve the integrity of the special beaks and the hinge. Complete drying is necessary before sterilization to avoid any trace of oxidation. Regular lubrication of the joint with an oil suitable for surgical instruments is recommended to maintain the flexibility of the EXLOG® mechanism.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a German company recognized for its expertise in the production of high-precision dental and surgical instrumentation. Although the specific regulatory class and CE marking are not detailed in the source data, Helmut Zepf products are designed to meet the technical requirements of healthcare professionals. The practitioner is invited to refer to the marking applied directly to the 15.222.00D instrument and to consult the accompanying instructions provided by the manufacturer to verify the certificates of conformity in force at the time of purchase, in accordance with European medical device regulations.

State of the art

Surgical medical consumables play a decisive role in operative safety.