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Spatula Hollenbach Number 1/2 with Handle Number 6 - Hu-Friedy - Delynov

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The Brunissoir Kotschy #13 - 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.

56.25 € 56.25 EUR 56.25 € Tax Included

56.25 € Tax Included

(0.00 € / Units)
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Instrument

What is the Kotschy #13 Burnisher - Hu-Friedy?

The Kotschy #13 Burnisher, manufactured by Hu-Friedy Mfg. Co., LLC, is a precision manual instrument belonging to the category of consumables for restorative dentistry. This burnishing instrument is specifically designed for the final shaping and smoothing of filling materials. As a Class I medical device, it meets the regulatory requirements for use in dental practices. Its structure is optimized to allow the practitioner to exert controlled pressure on restorative materials, thereby facilitating the achievement of a smooth and homogeneous surface before complete hardening or during finishing phases.

What are the clinical indications for this instrument?

The clinical indications for the Hu-Friedy Kotschy #13 Burnisher primarily concern operative dentistry procedures. It is used as an amalgam polishing instrument to condense material against the cavity walls and to remove excess material at the margins. Its application also extends to the burnishing of metal matrices to restore interproximal contact points. In conservative surgery, this instrument is essential for perfecting occlusal anatomy and ensuring a smooth transition between the natural tooth and the restorative material, thus limiting post-operative bacterial plaque accumulation.

What are the technical characteristics of this instrument?

The Kotschy #13 Burnisher is distinguished by an ergonomic design specific to Hu-Friedy standards. Although the exact material specifications are not detailed, instruments in this range are developed by Hu-Friedy Mfg. Co., LLC to offer adequate resistance to mechanical stress during burnishing. The shape of the active tip, designated under the reference Kotschy #13, is designed to access different dental surfaces. Its classification as Class I confirms its status as a reusable non-invasive medical device, requiring a standard sterilization protocol between each patient in accordance with the manufacturer's instructions.

What are the contraindications for the use of the burnisher?

According to the data provided by the manufacturer Hu-Friedy, there are no specific medical contraindications listed for this instrument, other than those common to the use of metal instruments in the mouth. The use of the Kotschy #13 Burnisher is strictly reserved for qualified healthcare professionals. It is imperative not to use the instrument if it shows signs of corrosion, deformation, or metal fatigue, as this could compromise the integrity of the restoration or patient safety. The practitioner must systematically refer to the instructions for use before any clinical manipulation.

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

As it is a manual instrument and not an absorbable suture, the concept of resorption does not apply. However, the durability of the Hu-Friedy Kotschy #13 Burnisher depends on strict compliance with cleaning and sterilization protocols. After each amalgam polishing intervention, the instrument must be cleared of material residues before undergoing a disinfection and sterilization cycle in an autoclave. It is recommended to use non-corrosive cleaning solutions to preserve the surface condition of the steel and guarantee the effectiveness of the burnishing instrument over the long term, thus avoiding any premature alteration of the active tip.

Who is the manufacturer and what standards are respected?

The Kotschy #13 Burnisher is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a recognized manufacturer in the dental instrumentation sector for its compliance with quality standards. This product is classified as a Class I medical device. Although specific CE marking is not mentioned in the source data, compliance with current regulations for Class I devices is ensured by the manufacturer for safe market placement. Professionals must read the instructions carefully to ensure usage compliant with Hu-Friedy guidelines.


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Manufacturer Hu-Friedy
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