Osteotomy Bone-Pusher Number 3.32 Straight 3.2mm Cylindrical - Hu-Friedy - Delynov

What is the Bone-Pusher #3.32 straight 3.2mm cylindrical osteotome - Hu-Friedy?

The Bone-Pusher #3.32 osteotome is a specialized manual instrument designed by Hu-Friedy for oral and implant surgery procedures. This device is characterized by a cylindrical working end with a diameter of 3.2mm and a straight shank. It is primarily used as an osteotome to manipulate, compact, or displace bone tissue and graft materials. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets the quality requirements of a recognized manufacturer in the dental sector. Its robust design allows for efficient force transmission during bone condensation maneuvers necessary for recipient site preparation.

What are the clinical indications for this osteotome?

This instrument is indicated for bone surgery procedures where bone densification or displacement is required. In implantology, the Hu-Friedy Bone-Pusher osteotome is used to compact cancellous bone to improve primary implant stability. It is also employed during crestal approach sinus lift techniques to gently push bone filling material under the sinus membrane. Its 3.2mm cylindrical shape is particularly suited to drilling sites of corresponding diameter, allowing for precise fit and optimal control of the bone volume displaced during the implant preparation phase.

What are the technical characteristics of the instrument?

The Bone-Pusher #3.32 osteotome features precise technical specifications to meet surgeons' needs. It has a cylindrical active part with a 3.2mm diameter, ideal for standardized surgical protocols. Its straight configuration allows for axial force application, which is essential for vertical compaction. As a Hu-Friedy brand product, this instrument benefits from a rigorous finish ensuring reliable handling. It belongs to the reusable consumables (CONSO) category and is classified as a Class I medical device according to current regulations, ensuring its compliance for professional use in dental offices or hospital environments.

What are the contraindications for the use of this device?

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 clinical contraindications apply, particularly when the patient's health status or local bone quality does not allow for invasive surgical intervention. Although the raw MDR text does not list specific material-related contraindications, the practitioner must ensure the patient does not have hypersensitivity to common metallic components of surgical instruments. It is imperative to read the instructions for use carefully and follow sterilization protocols before any intervention to avoid cross-infection risks.

What are the precautions for use and maintenance?

Like any Class I bone surgery instrument, the Hu-Friedy osteotome requires rigorous maintenance. Before the first use and after each intervention, the device must be cleaned, disinfected, and sterilized in accordance with the manufacturer's instructions. The practitioner must inspect the 3.2mm cylindrical tip to check for any deformation or damage that could compromise the precision of the surgical gesture. During use, excessive force must be avoided to prevent any risk of unwanted bone fracture or damage to the instrument. Handling must remain precise and compliant with osteotomy techniques taught in oral and implant surgery.

Who is the manufacturer and what standards are met?

The instrument is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a globally recognized manufacturer for the quality of its surgical instrumentation. This product is listed as a Class I medical device. Compliance with this regulatory class indicates that the instrument meets the safety and performance requirements defined for non-invasive or transient-use invasive medical devices. Healthcare professionals should refer to the manufacturer's warnings and consult the instructions for use to ensure use in compliance with current safety standards within their clinical practice.

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