Bone-Pusher Osteotome #5.32 bayonet 3.2mm cylind. - Hu-Friedy - Delynov

What is the Osteotome Bone-Pusher #5.32 bayonet?

The Osteotome Bone-Pusher #5.32 bayonet is a precision surgical instrument manufactured by Hu-Friedy. This device is specifically designed for the manipulation of bone filling materials. Its structure is distinguished by a bayonet shape, offering better visibility and easier access to difficult-to-reach clinical areas. The working end is cylindrical with a diameter of 3.2mm, which allows for controlled pressure on the graft material. As a Hu-Friedy brand instrument, it meets the quality requirements of practitioners specialized in oral surgery and implantology for bone reconstruction phases.

What are the clinical indications for this instrument?

This instrument is indicated for oral surgery procedures requiring the compaction of bone substitute materials. It is particularly used during sinus lifts via crestal or lateral approaches to push the material under the sinus membrane. Its design also allows for use in post-extraction socket preservation or guided bone regeneration (GBR). The clinical objective is to ensure optimal density of the filling material in the recipient site to promote future osseointegration of implants. This Hu-Friedy device is exclusively reserved for use by qualified healthcare professionals.

What are the technical characteristics of the Bone-Pusher #5.32?

The Bone-Pusher #5.32 features precise technical specifications to meet the needs of modern implantology. Its main characteristic is its cylindrical tip with a diameter of 3.2mm, sized to fit standard drilling sites and bone cavities. The bayonet-shaped shaft is a major ergonomic asset, allowing for the bypassing of anatomical obstacles or adjacent teeth without obstructing the surgeon's visual field. This instrument is part of the Class I range of devices from the manufacturer Hu-Friedy Mfg. Co., LLC, guaranteeing compliance with rigorous manufacturing standards for non-invasive or minimally invasive manual instrumentation.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for duly trained healthcare professionals. Although specific data on medical contraindications are not detailed in the raw documentation, general contraindications to oral and implant surgery apply. The use of this instrument is prohibited outside of its intended use, namely the transport and compaction of bone materials. The practitioner must imperatively read the instructions for use carefully and check the condition of the instrument before any intervention to rule out any risk related to wear or deformation.

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

As a reusable and non-resorbable surgical instrument, the Osteotome Bone-Pusher #5.32 requires a rigorous sterilization and maintenance protocol after each use. Although the exact composition is not specified, Hu-Friedy instruments in this category must be cleaned, disinfected, and sterilized according to the manufacturer's instructions to ensure the asepsis of the surgical field. The 3.2mm tip should be handled with care to avoid any alteration of the cylindrical surface, which could compromise the precision of the bone compaction. A visual check before each surgical act is recommended to ensure the structural integrity of the bayonet.

Who is the manufacturer and what standards are respected?

The Osteotome Bone-Pusher #5.32 bayonet is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed as Class I in accordance with current regulations. Hu-Friedy is a globally recognized manufacturer in the dental sector for the quality of its instrumentation. The product is distributed by Delynov and must be used in accordance with the manufacturer's warnings. It is essential for users to refer to the provided instructions for use to comply with all safety and usage protocols intended by the American manufacturer to ensure patient safety.

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