Peri-implant luxation, 3mm curved tip instrument - Helmut Zepf (17.007.07TI) - Delynov

What is the Helmut Zepf 17.007.07TI peri-implant luxator?

The Helmut Zepf peri-implant luxator is a specific manual instrument designed for oral surgery procedures requiring the removal of an implant. This model, identified under reference 17.007.07TI, is distinguished by an active tip with a width of 3 mm. Its structure is optimized to be inserted into the peri-implant space to initiate separation between the implant and the surrounding tissue. Manufactured by Helmut Zepf Medizintechnik GmbH, this tool meets the handling requirements of practitioners during the delicate luxation phases before the final extraction of the implant device.

What are the clinical indications for this instrument?

This peri-implant instrument is primarily indicated during dental implant removal procedures in cases of implant failure, severe peri-implantitis, or the need for device replacement. It serves as an implantology luxator to break the interface between the bone or soft tissues and the implant surface. Its use occurs prior to the application of greater extraction forces, allowing for a targeted approach around the circumference of the implant platform. The practitioner uses this instrument to progressively mobilize the implant within its socket.

What are the technical characteristics of this instrument?

The Helmut Zepf 17.007.07TI instrument features precise technical characteristics adapted to peri-implant anatomy. It has a curved tip with a width of 3 mm, a standard dimension for accessing narrow contact zones. The curvature of the active end is designed to provide an optimal angle of attack during luxation, facilitating passage around the threads or the neck of the implant. The technical reference 17.007.07TI indicates a specific design from the Helmut Zepf Medizintechnik GmbH manufacturer's catalog, guaranteeing compatibility with standard sterilization protocols in dental surgery practices.

What are the contraindications for using this luxator?

The contraindications for using this implant luxator are related to the patient's general clinical conditions and the state of adjacent structures. Its use is discouraged if the residual bone thickness is insufficient to support the fulcrum points without risk of significant alveolar fracture. Furthermore, as with any metallic instrument, a known hypersensitivity to the material components (although not specified here, generally titanium alloys or steel depending on the TI range) must be taken into account. The instrument should not be used for functions other than peri-implant luxation to avoid any deformation of the 3 mm curved tip.

What are the maintenance and storage precautions?

As a non-resorbable instrument intended for repeated use, this Helmut Zepf luxator requires a rigorous decontamination and sterilization protocol after each procedure. The practitioner must regularly inspect the integrity of the 3 mm curved tip to detect any signs of wear, corrosion, or bending that could compromise its effectiveness during luxation. It is recommended to follow the cleaning instructions provided by Helmut Zepf Medizintechnik GmbH, particularly regarding the use of non-corrosive cleaning solutions and compliance with standard autoclave cycles to maintain the mechanical properties of the peri-implant instrument.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Helmut Zepf Medizintechnik GmbH, a recognized company in the field of dental surgical instrumentation. Although the exact regulatory class and specific CE marking are not detailed in the source data for this reference 17.007.07TI, Helmut Zepf products are generally designed according to high quality standards to meet the needs of implant surgery. For any precise information regarding compliance with the European Medical Device Regulation (MDR) or obtaining certificates of conformity, it is advisable to refer to the technical documentation provided by the manufacturer or to consult the instructions for use attached to the product.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.