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Sinus Curette #2, Black Line

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The Curette Sinus #2, Black Line 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.

154.35 € 154.35 EUR 154.35 € Tax Included

154.35 € Tax Included

(0.00 € / Units)
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Instrument

What is the Sinus #2 Curette, Black Line?

The Sinus #2 Curette, Black Line is a high-precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is distinguished by its specific Black Line finish, designed to optimize visual contrast in the mouth and minimize distracting reflections under operating lights. As an instrument in the INSTRU category, it is specifically structured to meet the requirements of advanced oral surgery. Its design allows for rigorous handling during critical phases of the intervention, guaranteeing the practitioner a reliable tool for managing soft tissues and fine bone structures.

What are the clinical indications for this instrument?

This instrument is primarily indicated for implant and oral surgery procedures, specifically for sinus floor elevation (sinus lift). The sinus lift curette is used to carefully detach the sinus membrane from the internal bone wall after the osteotomy. It is used in creating the space necessary for the placement of a bone substitute. Its use is strictly reserved for qualified healthcare professionals, in accordance with the recommendations of the manufacturer Hu-Friedy, to ensure patient safety during these delicate invasive maneuvers.

What are the technical characteristics of the Sinus #2 Curette?

The Sinus #2 Curette from the Black Line range features technical characteristics adapted to the anatomy of the maxillary sinus. Its morphology is designed to access hard-to-reach areas while maintaining optimal tactile control. The characteristic black coating of the Black Line series by Hu-Friedy not only improves visibility but also provides a resistant surface. As a Class I device, this instrument meets the rigorous manufacturing standards of Hu-Friedy Mfg. Co., LLC, located in Chicago, ensuring compliance with regulatory requirements for non-invasive or short-term surgically invasive medical devices.

What are the contraindications for the use of this instrument?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is exclusively reserved for trained healthcare professionals. General clinical contraindications apply, particularly in cases of active sinus pathologies, untreated local infections, or systemic contraindications to oral surgery. It is imperative to read the instructions carefully before use to identify any specific restrictions related to the patient's health status or the planned surgical technique. Compliance with sterilization protocols is also a sine qua non condition to avoid any post-operative complications.

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

As a reusable surgical instrument made of steel or metal alloy, the Sinus #2 Curette requires a strict decontamination and sterilization protocol after each use. Although composition data is not detailed here, Hu-Friedy instruments must be maintained according to the manufacturer's specific instructions to preserve the integrity of the Black Line coating. Practitioners must inspect the instrument before each intervention to detect any signs of wear or degradation. Careful handling is recommended to avoid altering the working ends, which are essential for the safety of the sinus membrane during sinus elevation.

Who is the manufacturer and what standards are respected?

The Sinus #2 Curette is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device belongs to Class I according to the current regulatory classification. Hu-Friedy is a recognized manufacturer in the dental sector for its compliance with high quality standards. Although specific CE marking is not mentioned in the source data, the product follows strict directives relating to Class I medical devices. Healthcare professionals should refer to the labeling and instructions for use to confirm the certifications applicable to their geographic region.


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Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
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