Osteotomy Bone Spreader Number 4.32 Convex Bayonet 3.2mm - Hu-Friedy - Delynov

What is the Bone-Spreader #4.32 convex bayonet 3.2mm Osteotome?

The Bone-Spreader #4.32 Osteotome is a precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is distinguished by its convex working part and bayonet configuration, specifically designed for bone surgery interventions. With a diameter of 3.2mm, this tool is designed to meet the requirements of practitioners during the implant site preparation phases. As a Hu-Friedy brand product, this instrument benefits from the expertise of a manufacturer recognized in the field of medical instrumentation. It belongs to the consumables (CONSO) category and complies with the rigorous manufacturing standards imposed for devices of its class.

What are the clinical indications for this instrument?

The purchase of a surgery osteotome such as the Bone-Spreader #4.32 model is indicated for ridge expansion procedures and implant preparation in oral surgery. Its primary use consists of progressively widening the alveolar bone through lateral compression, which optimizes bone density around the future implant. The convex shape is particularly suitable for pushing back bone walls without material removal, thus preserving the patient's bone capital. The bayonet design facilitates access to the posterior sectors of the oral cavity, offering better visibility and an optimal approach angle for the dental surgeon or implantologist during condensation or expansion maneuvers.

What are the technical characteristics of this osteotome?

The Hu-Friedy #4.32 osteotome features precise technical specifications to ensure maximum clinical efficacy. It has a convex tip with a 3.2mm diameter, a critical dimension for the calibration of implant sites. Its bayonet-type structure is a major ergonomic asset, allowing for the bypass of anatomical obstacles and the application of controlled axial force. This device is classified as Class I according to medical device regulations. Manufacturing by Hu-Friedy ensures a high-quality finish, essential for instruments intended to be in direct contact with bone tissue. Every detail, from the curvature of the shaft to the shape of the tip, is designed to meet the strict protocols of modern oral surgery.

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. Contraindications include all clinical situations where bone surgery is prohibited or presents a major risk to the patient, in accordance with standard implantology protocols. It is imperative to refer to the specific indications and contraindications provided by Hu-Friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. The practitioner must evaluate the patient's bone density and systemic health before any intervention. Inappropriate use by an untrained person can lead to surgical complications. It is therefore essential to read the instructions carefully before use.

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

As a metallic surgical instrument and not a resorbable device, the precautions for use mainly concern maintaining the integrity of the instrument and patient safety. Before each intervention, the practitioner must check the condition of the 3.2mm convex tip to ensure the absence of deformations or damage. Although exact material details are not specified in the source data, this type of Hu-Friedy instrument requires rigorous cleaning, disinfection, and sterilization between each patient, in accordance with current asepsis protocols. Compliance with the sterilization cycles recommended by the manufacturer is essential to guarantee the tool's longevity and prevent any risk of cross-contamination during the osteotome surgery purchase.

Who is the manufacturer and what standards are respected?

The Bone-Spreader #4.32 Osteotome is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed as Class I, which corresponds to the safety and performance standards for this category of surgical instruments. As a recognized manufacturer, Hu-Friedy ensures that its products meet strict regulatory requirements for professional use in clinical settings. Although specific CE marking is not mentioned in the current technical sheet, compliance with Class I standards guarantees rigorous quality control. Practitioners are invited to consult the instructions for use to become familiar with all warnings and safety directives provided by the manufacturer.

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