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Osteotome Bone-Pusher #3.27 straight 2.7mm cylindrical - Hu-Friedy - Delynov

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The Ostéotom Bone-Pusher #3.27 droit 2.7mm 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 Bone-Pusher #3.27 straight 2.7mm cylindrical osteotome - Hu-Friedy?

The Bone-Pusher #3.27 osteotome from the Hu-Friedy brand is a manual surgical instrument specifically developed for implantology and oral surgery interventions. This device features a cylindrical working part with a diameter of 2.7mm and a straight shank. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument is designed to manipulate, compact, and position bone graft materials or natural bone in precise surgical areas. Its rigid structure allows for efficient force transmission during bone condensation maneuvers, thus ensuring reliable handling for the practitioner.

What are the clinical indications for this osteotome?

The use of this Hu-Friedy instrument is primarily indicated during pre-implant surgeries requiring bone density management or the addition of filling material. It is used for lateral or apical bone compaction, particularly in implant site preparation techniques where expansion or condensation of cancellous bone is required. In sinus surgery, it facilitates the pushing of graft material under the Schneiderian membrane after a crestal osteotomy. Its 2.7mm diameter makes it suitable for medium-sized sites, allowing for targeted application without compromising the integrity of surrounding structures.

What are the technical characteristics of this instrument?

The Bone-Pusher #3.27 osteotome is characterized by a cylindrical tip calibrated at 2.7mm, offering a flat contact surface for uniform pushing of the material. The straight design of the instrument is ideal for direct access, particularly in anterior sectors or easily accessible maxillary areas. As a Class I device, it meets standard manufacturing requirements for reusable surgical instruments. Hu-Friedy's manufacturing quality ensures mechanical resistance adapted to the stresses of manual bone condensation, while allowing for sterilization in accordance with standard hospital and clinical protocols.

What are the contraindications for the use of this device?

In accordance with information from the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. General clinical contraindications include situations where bone density is insufficient to support mechanical pressure or when the local anatomy presents a risk of unintended perforation (nerve or sinus proximity without visual control). Although the raw MDR text does not list specific medical contraindications related to the material, it is imperative to refer to the instructions for use before any intervention to validate the suitability of the instrument with the patient's health status.

What are the precautions for use and maintenance?

As a Class I surgical instrument, the Hu-Friedy Bone-Pusher osteotome requires a strict protocol for cleaning, disinfection, and sterilization between each patient. It is essential to check the integrity of the 2.7mm cylindrical tip before each use to ensure the absence of deformations or residues. The practitioner must adapt the force applied during compaction to avoid any fracture of the alveolar walls or damage to soft tissues. Careful reading of the instructions provided by the manufacturer Hu-Friedy, located in Chicago, USA, is mandatory to guarantee patient safety and the longevity of the instrument.

Who is the manufacturer and what standards are respected?

The osteotome is manufactured by Hu-Friedy Mfg. Co., LLC, a recognized company in the field of dental instrumentation, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device. The manufacturer emphasizes that the use of this instrument is exclusively reserved for healthcare professionals trained in oral surgery techniques. Compliance with manufacturing standards ensures that the instrument meets safety and performance requirements for its intended use in a clinical environment. For any additional information, it is recommended to consult the official technical documentation from Hu-Friedy.


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Manufacturer Hu-Friedy
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