Exlog surgical dental extraction forceps, model fig. 36M - Helmut Zepf (15.236.08) - Delynov

What is the Exlog surgical forceps, model fig. 36M?

The Exlog surgical forceps model fig. 36M is a high-precision extraction instrument developed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device, bearing the technical reference 15.236.08, belongs to the Exlog range, recognized for its optimized design facilitating avulsion procedures. As an instrument in the CONSO category at Delynov, it is intended for dental surgeons and oral surgery specialists for the safe handling of hard tissues during extraction phases. Its structure is specifically designed to provide a reliable interface between the practitioner's hand and the tooth, ensuring controlled force transmission.

What are the clinical indications for this Helmut Zepf forceps?

This surgical forceps is indicated for dental extraction within the framework of oral surgery, periodontology, or pre-implant surgery protocols. The fig. 36M model is used to firmly grasp the tooth or root to perform luxation and avulsion movements. Its use is particularly relevant during surgeries requiring reliable Helmut Zepf instrumentation to minimize the risk of root fracture or damage to the surrounding alveolar tissues. It fits perfectly into the technical tray of implantologists during immediate extraction-implantations where preserving the integrity of the bone plate is paramount.

What are the technical characteristics of the model 15.236.08?

The Helmut Zepf forceps reference 15.236.08 is distinguished by its Exlog design, which aims to improve the ergonomics and efficiency of the surgical gesture. Although detailed material specifications are not explicitly listed, instruments in this range are designed to meet the severe mechanical constraints of avulsion. The fig. 36M configuration defines the geometry of the beaks and the angulation of the handles, allowing targeted access according to the position of the tooth in the arch. The surface finish and hinge adjustment ensure smooth handling and durability in accordance with the manufacturing standards of Helmut Zepf Medizintechnik GmbH.

What are the contraindications for the use of this instrument?

Contraindications to the use of the Exlog fig. 36M forceps are mainly related to clinical situations where a classic instrumental extraction is deemed risky or impossible. This includes cases of extreme bone fusion (ankylosis) requiring a prior alveolotomy approach, or situations where the patient presents general contraindications to oral surgery (uncontrolled hemostasis disorders, serious systemic pathologies). It is imperative not to use the instrument for unintended purposes, such as handling non-biological materials, which could damage the beaks or the hinge. The practitioner must evaluate the residual strength of the dental crown before applying force.

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

As a reusable metal surgical instrument, the Helmut Zepf forceps must undergo a rigorous decontamination, cleaning, and sterilization protocol after each use. It is recommended to follow the specific instructions from the manufacturer Helmut Zepf Medizintechnik GmbH regarding autoclave cycles and compatible cleaning products to avoid any corrosion or alteration of the steel. Particular attention must be paid to the hinge of model 15.236.08 to ensure the absence of organic residues. A visual check of the beak alignment and surface condition is recommended before each intervention to ensure patient safety and the effectiveness of the procedure.

Who is the manufacturer and what standards are respected?

The surgical forceps of the Exlog range is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of high-quality dental and surgical instrumentation. Although the exact regulatory class and specific CE marking are not mentioned in the current source documentation, this product is designed according to the rigorous German manufacturing standards associated with the Helmut Zepf brand. Healthcare professionals are invited to refer to the product labeling and the instructions for use provided by Delynov to verify the current compliance certifications and safety instructions related to the Medical Device Regulation (MDR).

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