Osteotomy Bone Pusher Number 3.42 Straight 4.2mm Cylindrical - Hu-Friedy - Delynov

What is the Osteotome Bone-Pusher #3.42straight 4.2mm cylindrical - Hu-Friedy?

The Osteotome Bone-Pusher #3.42straight is a specialized manual instrument developed by the manufacturer Hu-Friedy. This device is characterized by a cylindrical tip with a diameter of 4.2mm and a straight shank. It is designed to manipulate, push, and compact graft materials or bone tissue during surgical interventions. Its rigid structure allows for precise axial force transmission, essential for the preparation of recipient sites in implantology. As a product of the Hu-Friedy brand, it benefits from the manufacturing expertise of Hu-Friedy Mfg. Co., LLC, guaranteeing an instrument adapted to the clinical requirements of oral surgery operating rooms.

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

The clinical indications for this osteotome bone-pusher primarily concern implant surgery and bone reconstruction. It is used by healthcare professionals for bone compaction during ridge expansion or for pushing filling biomaterials. Its 4.2mm cylindrical shape is particularly suited to drilling sites of corresponding diameter, allowing for homogeneous condensation of the graft material. The intended use, as defined by Hu-Friedy Mfg. Co., LLC, limits the use of this instrument to qualified practitioners performing oral surgery protocols requiring precise manipulation of bone structures.

What are the technical characteristics of the Osteotome Bone-Pusher #3.42straight?

Technically, this Hu-Friedy instrument features a cylindrical working part with a 4.2mm diameter. Its straight configuration (#3.42straight) facilitates direct access to maxillary or mandibular sectors without angular obstruction. The tip design is optimized for pressure transfer without excessive trauma to the surrounding bone walls. Manufactured by Hu-Friedy Mfg. Co., LLC, this tool meets Class I quality standards. The precision of the 4.2mm diameter allows the surgeon to work in alignment with drills and implants of similar dimensions, ensuring a perfect match during bone condensation stages.

What are the contraindications for the use of this device?

According to information from the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for trained healthcare professionals. Contraindications include use in clinical situations where the patient's physiological conditions do not allow for bone surgery (uncontrolled systemic pathologies, local irradiation). It must not be used for functions other than those intended by the manufacturer, such as excessive leverage that could damage the instrument or anatomical structures. The practitioner must refer to the instructions for use and evaluate the specific risks for each patient before any intervention with this Class I osteotome.

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

As a reusable metal surgical instrument, and not a resorbable device, the Hu-Friedy Osteotome Bone-Pusher requires a rigorous sterilization protocol between each patient. Although the exact composition is not specified, the maintenance of this type of Class I instrument involves pre-disinfection cleaning, thorough rinsing, and autoclave sterilization according to parameters validated by Hu-Friedy Mfg. Co., LLC. It is imperative to check the integrity of the 4.2mm cylindrical tip before each use to detect any signs of wear or deformation that could compromise the precision of the surgical gesture or patient safety.

Who is the manufacturer and what standards are met by this product?

The Osteotome Bone-Pusher #3.42straight is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed in the CONSO category and belongs to Class I according to current regulations. As a recognized manufacturer in the dental sector, Hu-Friedy guarantees that this instrument is intended exclusively for professional use. Although specific CE marking is not mentioned in the source data, compliance with Class I standards ensures that the product meets the safety and performance requirements for manual non-invasive or short-term invasive surgical instruments.

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