Gracey Curette n°11/12 handle n°7 orange mesial - Hu-Friedy - Delynov

What is the #242 Goldstein interproximal excavator - Hu-Friedy - Delynov?

The #242 Goldstein interproximal excavator is a precision manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. This medical device belongs to the category of consumables (CONSO) and is specifically designed for interventions in interproximal areas. Its structure allows for rigorous handling during conservative or surgical care. As an instrument from the Hu-Friedy brand, it benefits from the expertise of a recognized manufacturer in the dental and surgical instrumentation sector. This Goldstein model is particularly suited to the needs of practitioners requiring a reliable tool for treating dental surfaces and restricted spaces.

What are the clinical indications for this interproximal excavator?

The intended use of this interproximal excavator primarily concerns restorative surgery and periodontal care. It is indicated for the precise removal of debris, decayed tissue, or excess materials located in interproximal spaces. Dental surgeons use this Hu-Friedy instrument to access areas where standard excavators would be too bulky. It facilitates the cleaning of prepared cavities and allows for meticulous adjustment of restorative materials before they harden. In accordance with the manufacturer's guidelines, its use is strictly reserved for qualified healthcare professionals working in dental offices or hospital settings.

What are the technical characteristics of this device?

The #242 Goldstein interproximal excavator stands out for its design focused on access to narrow areas. Manufactured by Hu-Friedy, this instrument meets Class I quality standards. Although the composition specifications are not detailed in the source data, the Goldstein range is recognized for the thinness of its active tips, allowing for non-invasive intervention in the interdental septum. Its interproximal configuration ensures effective transmission of tactile force, essential for differentiating healthy tissue from pathological tissue or for manipulating filling materials with great technical accuracy during clinical phases.

What are the contraindications for the use of this instrument?

According to the information provided by Hu-Friedy Mfg. Co., LLC, specific contraindications are not listed exhaustively beyond standard warnings. However, the use of this excavator is contraindicated for any person who does not have the required professional qualification, as it is exclusively reserved for healthcare professionals. The instrument should not be used outside of its intended use, namely intervention in the interproximal zone. The practitioner must systematically consult the instructions for use before use to ensure the instrument's suitability for the patient's clinical condition and the absence of specific risks related to the planned procedure.

What are the precautions for use and maintenance?

Like any Class I instrument intended for oral surgery, the #242 Goldstein excavator must be handled with care. Although resorption does not apply to this non-resorbable metallic instrument, precautions primarily concern sterilization and inspection before use. The manufacturer Hu-Friedy emphasizes the importance of carefully reading the instructions to ensure patient safety and tool longevity. It is imperative to check the integrity of the active parts before each intervention. Compliance with the cleaning and disinfection protocols recommended by the manufacturer is essential to maintain the performance of the interproximal excavator throughout its life cycle.

Who is the manufacturer and what standards are respected?

The #242 Goldstein interproximal excavator is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered 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 a major and recognized player in the production of high-quality surgical instruments. The product is distributed by Delynov and must be used in accordance with the indications and warnings provided by the manufacturer. Although CE marking is not specified in the source data, compliance with Class I requirements ensures that the instrument meets essential safety standards for professional use in a medical environment.

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