Surgical dental extraction forceps for children, English pattern Figure 51, Roba design - Helmut Zepf (10.685.51ZD) - Delynov

What is the Helmut Zepf 10.685.51ZD surgical forceps for children?

The surgical forceps for children referenced 10.685.51ZD is a specialized instrument designed by Helmut Zepf Medizintechnik GmbH. This model is based on the classic configuration of the English model figure 51, reworked according to the Roba design. It is a pediatric dental instrument specifically sized to meet the anatomical constraints of young patients. Its structure is optimized to offer a secure grip while respecting the limited space of the infantile oral cavity. This device is part of the standard consumption range (CONSO) for practices performing pediatric oral surgery.

What are the clinical indications for these pediatric surgery forceps?

These pediatric surgery forceps are primarily indicated for the extraction of temporary teeth or roots in children. Its use is recommended during orthodontic treatments requiring guided avulsions or in cases of irreversible infectious pathologies affecting the deciduous dentition. The Roba design, combined with the figure 51 of the English model, allows the surgeon to apply the necessary forces for luxation and extraction with controlled force transmission. It is used daily by pedodontists and dental surgeons during simple or complex exodontia procedures in young subjects.

What are the technical characteristics of the 10.685.51ZD model?

The technical characteristics of these pediatric dental surgery forceps are based on the expertise of Helmut Zepf in precision instrumentation. This model bears the technical reference 10.685.51ZD and is distinguished by its Roba design, which modifies the geometry of the beaks for better adaptation to pediatric dental necks. The English model figure 51 configuration defines the orientation and curvature of the instrument, facilitating access to posterior or anterior areas depending on the specific angulation. Although exact dimensions are not listed, its design is inherently linked to pediatric extraction standards, guaranteeing a balance between compactness and mechanical efficiency.

What are the contraindications for the use of this instrument?

The contraindications for the use of these forceps are linked to standard exodontia protocols. It must not be used on permanent adult dentition if the size of the beaks is not compatible with the crown volume, at the risk of fracturing the tooth or damaging the instrument. As with any metallic instrument, its use is prohibited in patients with a known hypersensitivity to the metals constituting the alloy, even though it is of medical grade. A prior clinical evaluation of the residual strength of the tooth and the proximity of permanent tooth germs is essential before any application of this instrument.

What are the maintenance and durability precautions for these pediatric forceps?

As a non-resorbable and reusable instrument, these pediatric extraction forceps require a rigorous sterilization protocol after each intervention. Precautions include pre-disinfectant cleaning, use of an ultrasonic bath if necessary, and sterilization in an autoclave according to the cycles validated by the manufacturer Helmut Zepf Medizintechnik GmbH. The absence of corrosion or deformation at the joint and beaks should be checked regularly. Proper maintenance guarantees the longevity of the instrument and prevents risks of cross-contamination, thus ensuring the safety of the patient and the practitioner during repetitive surgical acts.

Who is the manufacturer and what standards are respected by these forceps?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, a recognized player in the field of high-precision dental instrumentation. Manufacturing follows the rigorous quality standards specific to the German industry. Although the specific regulatory class and CE marking are not detailed in the technical documentation provided, this device is designed to meet the professional requirements of dental surgery. Practitioners are invited to refer to the instructions for use and the markings on the packaging to confirm current certifications and maintenance instructions specific to the 10.685.51ZD model.

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