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Osteotomy Bone Pusher No. 5.42 Bayonet 4.2mm Cylindrical - Hu-Friedy

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The Pousseur d'os d'ostéotomie n° 5.42 Baïonnette 4,2mm 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 Osteotomy Bone Pusher No. 5.42 Bayonet 4.2mm?

The Osteotomy Bone Pusher No. 5.42 Bayonet is a specialized instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is distinguished by its specific bayonet-shaped structure, designed to offer increased visibility and access during complex surgical interventions. It features a cylindrical tip with a diameter of 4.2mm. As a bone condensation instrument, it primarily serves to manipulate and compact bone tissue or substitute materials. This product belongs to the surgical consumables category and benefits from the expertise of Hu-Friedy, a recognized manufacturer in the field of precision instrumentation for oral and implant surgery.

What are the clinical indications for this Hu-Friedy instrument?

This instrument is indicated for osteotomy procedures and implant site preparation. It is used by dental surgeons and implantologists for bone condensation, a crucial step to improve local density before placing an implant. Its design allows for the controlled displacement of bone, particularly in cases of crestal sinus lifts or ridge expansion. The use of this dental bone pusher is strictly reserved for qualified healthcare professionals, in accordance with Hu-Friedy manufacturer guidelines. It is used in oral surgery protocols requiring precise management of bone volumes and densification of recipient sites.

What are the technical characteristics of the Bone Pusher No. 5.42?

The Bone Pusher No. 5.42 features precise technical specifications to meet the requirements of bone surgery. It is equipped with a cylindrical tip with a diameter of 4.2mm, allowing for the application of force distributed over a defined surface. Its bayonet shape is a major ergonomic feature, offsetting the handle axis relative to the working part to prevent obstruction of the visual field by the practitioner's hand or the instrument itself. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets the brand's quality standards. It is classified as a Class I medical device, guaranteeing its compliance with basic regulatory requirements for non-invasive or short-term invasive reusable surgical instruments.

What are the contraindications for the use of this instrument?

According to information provided by the manufacturer Hu-Friedy, the use of this instrument is reserved exclusively for healthcare professionals. General clinical contraindications apply, including use on patients with uncontrolled systemic pathologies that contraindicate oral or implant surgery. It must not be used for functions other than those intended, such as the application of excessive leverage forces that could damage the bone or the instrument. The practitioner must carefully consult the instructions before use to ensure the device is appropriate for the patient's specific clinical situation and the planned operative protocol.

What are the precautions for use and maintenance?

As a Class I instrument manufactured by Hu-Friedy, it must be handled with care to maintain the integrity of its 4.2mm cylindrical tip. Before each use, the healthcare professional must carefully read the instructions. Although sterilization details are not specified in the source data, these metallic instruments generally require rigorous cleaning and sterilization between each patient to prevent cross-contamination. It is imperative to check the condition of the instrument before the surgical act to detect any signs of wear or deformation. Compliance with the maintenance protocols recommended by Hu-Friedy Mfg. Co., LLC ensures the longevity and safety of the instrument during bone condensation phases.

Who is the manufacturer and what standards are met?

The Osteotomy Bone Pusher No. 5.42 is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered in Chicago, Illinois, USA. This medical device is classified as Class I according to current regulations. The manufacturer emphasizes that the use of this instrument is strictly reserved for healthcare professionals. Compliance with Class I standards indicates that the product meets the essential safety and performance requirements defined for this category of surgical instruments. Hu-Friedy is a globally recognized manufacturer for the rigor of its manufacturing processes, guaranteeing practitioners a reliable tool for their daily interventions in implant and periodontal surgery.


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Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Hu-Friedy
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