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Osteotom Bone-Pusher #3.50 straight 5.0mm cylindrical - Hu-Friedy - Delynov

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The Ostéotom Bone-Pusher #3.50 droit 5.0mm cylindrique - Hu-Friedy is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.

  • Compliance: Medical device Class I.
  • Manufacturer: Hu-Friedy Mfg. Co., LLC.
  • Reserved for healthcare professionals. Read instructions carefully before use.

55.50 € 55.5 EUR 55.50 € Tax Included

55.50 € Tax Included

(0.00 € / Units)
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Instrument

What is the Bone-Pusher #3.50 straight Osteotome?

The Bone-Pusher #3.50 straight Osteotome is a precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. It features a cylindrical-shaped tip with a diameter of 5.0mm and a straight shank. This device is specifically designed for bone condensation steps in implantology. As a straight osteotome, it allows the practitioner to exert direct axial force to manipulate filling materials. This equipment belongs to the consumables category (CONSO) and benefits from the expertise of Hu-Friedy, a recognized manufacturer in the field of dental instrumentation. Its robust structure meets the requirements of operating rooms for complex oral surgeries requiring rigorous bone compaction.

What are the clinical indications for this straight dental osteotome?

The purchase of a Bone-Pusher type dental osteotome is primarily indicated during pre-implant and implant surgery procedures. Its major clinical role is to compact bone graft materials (autologous, allogenic, or synthetic) into recipient sites. It is particularly used during crestal sinus lift techniques, where it serves to gently push the filling material under the previously detached sinus membrane. Its 5.0mm cylindrical tip ensures a homogeneous distribution of pressure, thus promoting the primary stability of the future implant. This instrument is reserved exclusively for health professionals trained in oral surgery and implantology techniques.

What are the technical characteristics of this instrument?

The Bone-Pusher #3.50 osteotome features precise technical specifications to meet the needs of surgeons. It has a cylindrical active part with a 5.0mm diameter, a dimension suitable for standard to wide implant sites. The straight configuration of the instrument allows for optimal transmission of manual force in the axis of the osteotomy, which is essential for vertical bone condensation. Manufactured by Hu-Friedy, this device benefits from a high-quality finish specific to the brand's standards. It is classified as a Class I medical device according to current regulations. Its ergonomic design aims to provide a stable grip during critical phases of hard tissue manipulation.

What are the contraindications for the use of this dental bone pusher?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. General contraindications include any clinical situation where bone surgery is proscribed, such as uncontrolled systemic pathologies affecting bone healing or active local infections at the surgical site. Although technical documents do not list specific material-related contraindications, it is the practitioner's responsibility to verify the suitability of the instrument with the patient's bone density and the surgical technique employed. It is imperative to carefully read the instructions for use and respect the warnings from the manufacturer located in Chicago, USA, before any intervention.

What are the precautions for use and maintenance?

The use of the Bone-Pusher #3.50 osteotome requires careful handling to avoid any fracture of the bone walls or unwanted perforation, particularly during maneuvers near the maxillary sinus. Before each use, the professional must inspect the integrity of the 5.0mm cylindrical tip. As a Class I instrument, it must be cleaned, disinfected, and sterilized according to standard hospital protocols and specific Hu-Friedy instructions to ensure asepsis. The precision of the straight osteotome depends on maintaining its surface condition and the absence of deformation. Compliance with the sterilization cycles recommended by the manufacturer Hu-friedy 3232 N. Rockwell St. Chicago is essential to preserve the mechanical properties of the instrument over the long term.

Who is the manufacturer and what standards are met?

The device is manufactured by Hu-Friedy Mfg. Co., LLC, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is a Class I medical device. Hu-Friedy is a globally recognized manufacturer for the quality and reliability of its dental surgery instruments. Compliance with Class I indicates that the instrument meets the basic regulatory requirements for non-invasive or temporary-use invasive medical devices. Practitioners must systematically refer to the provided instructions for use to ensure the compliance of reprocessing and clinical use procedures. Hu-Friedy's traceability and manufacturing quality ensure optimal safety for dental surgeons and their patients.


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Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Hu-Friedy
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