Osteotomy bone pusher No. 3.37 right 3.7mm cylindrical - Hu-Friedy - Delynov

What is the Osteotome Bone-Pusher #3.37 straight 3.7mm?

The Osteotome Bone-Pusher #3.37 straight 3.7mm is a precision instrument manufactured by Hu-Friedy, a recognized player in the medical device sector. This device is characterized by a straight cylindrical tip with a diameter of 3.7mm. It is specifically designed to manipulate and condense bone graft materials within surgical sites. Its rigid structure allows for controlled force transmission during critical stages of implant surgery. As a manual instrument, it offers the practitioner essential tactile feedback to assess bone density and resistance during the insertion of filling materials.

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

The clinical indications for this Hu-Friedy instrument focus primarily on oral surgery and implantology. It is used when purchasing dental surgery instruments for crestal approach sinus floor elevation techniques (Summers technique). Its role is to compact the bone filling material (autologous, allogenic, or synthetic) in order to gradually lift the Schneiderian membrane. It can also be employed in other situations requiring localized bone condensation or the displacement of hard tissues in cylindrical cavities of corresponding diameter, thus guaranteeing a stable base for subsequent implant placement.

What are the technical characteristics of this osteotome?

Technically, this osteotome features a straight configuration, ideal for anterior sectors or direct access zones. The working part is cylindrical with a diameter calibrated at 3.7mm, which corresponds to the standards of drilling sequences in implantology. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument benefits from a high-quality finish specific to the brand's standards. Its design allows for repeated sterilization in an autoclave, respecting the strict hygiene protocols of dental practices. The reference #3.37 specifies its place in the manufacturer's range of bone condensation instruments.

What are the contraindications for the use of this device?

According to the information provided by Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. Contraindications include any clinical situation where bone surgery is prohibited, such as uncontrolled systemic pathologies affecting bone healing or active local infections at the surgical site. The use of the instrument on an anatomical structure unsuitable for the 3.7mm diameter or without prior radiological planning is also contraindicated. It is imperative to carefully read the manufacturer's instructions before any use to ensure the compatibility of the surgical procedure with the patient's health status.

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

As a reusable and non-resorbable surgical instrument, precautions for use are based on maintaining its physical integrity and sterility. After each intervention, the Osteotome Bone-Pusher must be cleaned, decontaminated, and sterilized in accordance with Hu-Friedy instructions. The practitioner must inspect the 3.7mm cylindrical tip before each use to detect any trace of wear, corrosion, or deformation that could compromise the precision of the procedure or patient safety. Prudent handling is required when applying impaction forces to avoid any accidental perforation of the sinus membrane or fracture of the alveolar walls.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device, meeting the basic regulatory requirements for manual surgical instruments. Although specific CE marking is not mentioned in the source data, compliance with Hu-Friedy manufacturing standards ensures consistent quality. The use of this instrument is exclusively reserved for healthcare professionals trained in oral surgery techniques. Strict adherence to the manufacturer's warnings and the instructions for use is essential to ensure regulatory compliance within the practice.

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