EXLOG® DENTAL EXTRACTION FORCEPS FIG. 35M ROBA FOR UPPER PREMOLARS - Helmut Zepf (15.235.08) - Delynov

What is the Helmut Zepf EXLOG® FIG. 35M forceps?

The EXLOG® FIG. 35M forceps, referenced under code 15.235.08, is a manual oral surgery instrument manufactured by Helmut Zepf Medizintechnik GmbH. This device belongs to the EXLOG® range, recognized for its high manufacturing standards. It is a metallic instrument designed for the firm gripping of dental structures during exodontia procedures. Its morphology is specifically adapted to the anatomy of upper premolars, allowing for optimal transmission of forces during the rotation and traction movements required for avulsion.

What are the clinical indications for this instrument?

This forceps is exclusively indicated for the extraction of premolars located in the upper maxilla. In clinical practice, it is used during exodontia surgeries for reasons such as non-restorable caries, root fractures, or as part of orthodontic treatment plans requiring extractions. Oral surgery and implantology practitioners use this Helmut Zepf instrument to mobilize the tooth after syndesmotomy, thus facilitating the removal of the dental organ while preserving the integrity of the surrounding alveolar bone plates.

What are the technical characteristics of the 15.235.08 forceps?

The Helmut Zepf EXLOG® FIG. 35M forceps features a precise anatomical configuration for upper premolars. Its beaks are designed to adapt to the cervical curvature of these teeth, ensuring a stable grip without excessive slipping. The technical reference 15.235.08 corresponds to a specific design in the EXLOG® range, characterized by a refined finish facilitating cleaning and decontamination. The structure of the instrument is designed to withstand repeated mechanical stress during sterilization cycles and daily surgical interventions in the dental office.

What are the contraindications for the use of this device?

There are no specific documented medical contraindications for the use of this forceps, other than general contraindications related to any oral surgery procedure (uncontrolled coagulation disorders, serious systemic pathologies, or recent local irradiation). The instrument must not be used on teeth for which it is not designed, such as molars or mandibular teeth, at the risk of damaging soft tissues or causing a root fracture due to poor adaptation of the beaks.

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

As it is a reusable metal surgical instrument, the Helmut Zepf forceps requires a strict sterilization protocol between each patient. After the procedure, it must be pre-disinfected, cleaned (manually or by ultrasound), and rinsed before being placed in a pouch for autoclave sterilization. It is important to check for the absence of organic debris in the hinges and on the beaks before the thermal cycle. Compliance with the recommendations of the manufacturer Helmut Zepf Medizintechnik GmbH regarding cleaning products is essential to maintain the integrity of the instrument.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a German company specializing in high-precision dental surgical instrumentation. Although specific regulatory class and CE marking data are not detailed in this technical sheet, Helmut Zepf products are manufactured according to rigorous quality standards specific to European medical devices. For any precise information on regulatory compliance or current ISO certifications, it is recommended to refer to the instructions for use or technical documents provided by the manufacturer.

State of the art

Surgical medical consumables play a decisive role in operative safety.