Skip to Content

Sinus Lift Elevator Curette number 914 with short handle number 10 - Hu-Friedy - Delynov

https://www.delynov.fr/web/image/product.template/24935/image_1920?unique=0fe73e7

The Curette élévation sinusale #914 manche #10 court - 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.

138.45 € 138.45 EUR 138.45 € Tax Included

138.45 € Tax Included

(0.00 € / Units)
  • Manufacturer

This combination does not exist.

Instrument

What is the Hu-Friedy sinus lift curette #914?

The sinus lift curette #914 is a manual surgical instrument developed by the manufacturer Hu-Friedy Mfg. Co., LLC. This device is distinguished by its specific structure including a short #10 handle, optimized for interventions requiring increased maneuverability in restricted spaces. As a sinus lift instrument, it is intended for the manipulation of soft tissues during sub-sinus bone grafting procedures. Its design meets the rigorous requirements of implant and oral surgery practitioners, ensuring a precise interface between the instrument and the sinus membrane.

What are the clinical indications for this instrument?

The use of this sinus lift instrument is strictly reserved for healthcare professionals qualified in oral surgery and implantology. The sinus lift curette #914 is primarily indicated for sinus lift protocols, where it is used for the elevation of the Schneiderian membrane after the osteotomy of the lateral wall of the maxillary sinus. It allows for the creation of the space necessary for the insertion of bone filling material. Its use is documented for clinical cases presenting insufficient residual bone height in the posterior maxilla, requiring volume augmentation before implant placement.

What are the technical characteristics of the #914 curette?

The Hu-Friedy sinus lift curette #914 features technical characteristics adapted to the anatomical constraints of the sinus. The specific #914 reference defines the curvature and orientation of the working ends for effective mucosal detachment. The short #10 handle is a major specificity, offering leverage and tactile control adapted to the practitioner's hands while limiting intraoral bulk. Manufactured by Hu-Friedy Mfg. Co., LLC, this Class I instrument is designed to undergo repeated sterilization cycles in accordance with standard hospital protocols, ensuring longevity consistent with the brand's standards.

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 subject to standard clinical indications and contraindications related to sinus surgery. General contraindications include acute sinus pathologies, untreated local infections, or any systemic condition of the patient preventing invasive surgical intervention. The manufacturer specifies that this device is exclusively reserved for healthcare professionals. It is imperative to carefully read the instructions for use provided by Hu-Friedy before any intervention to ensure the suitability between the instrument and the patient's clinical status.

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

As a reusable metallic instrument and not a resorbable device, the Hu-Friedy sinus lift curette #914 requires a rigorous decontamination and sterilization protocol after each use. Practitioners must follow manual or ultrasonic cleaning instructions before autoclaving. The integrity of the sinus lift instrument's working ends should be regularly inspected to detect any wear or deformation that could compromise the safety of the sinus membrane. Maintenance in compliance with Hu-Friedy manufacturer guidelines ensures the maintenance of technical performance and patient safety during surgical acts.

Who is the manufacturer and what standards are respected?

The sinus lift curette #914 is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. The manufacturer Hu-Friedy is globally recognized for the quality of its surgical instrumentation. Compliance with manufacturing standards ensures that the instrument meets the safety and performance requirements for use in a clinical setting. Professionals should refer to the labeling and instructions for use to confirm the regulatory specificities applicable at the time of purchase on Delynov.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
Tags
Tags
Instrument