Periodontal probe Goldman-Fox no. 23 with handle no. 6 - Hu-Friedy - Delynov

What is the Goldman-Fox #23 periodontal probe?

La sonde parodontale Goldman-Fox #23 est un instrument de diagnostic manuel. Ce dispositif se compose d'une extrémité de travail graduée et d'un manche #6. Il est spécifiquement développé pour les praticiens réalisant des examens parodontaux. Sa structure permet une exploration fine des tissus de soutien. En tant qu'instrument de mesure, il aide à quantifier l'espace entre la gencive et la surface, fournissant des données essentielles pour le suivi de la santé parodontale des patients. Sa conception répond aux exigences de qualité de Hu-Friedy Mfg. Co., LLC, assurant une fiabilité lors des procédures diagnostiques quotidiennes en chirurgie orale ou en parodontologie.

What are the clinical indications for this probe?

The goldman fox probe is indicated for the systematic clinical evaluation of the periodontium. It is used by the practitioner to measure the depth of the sulcus or pathological periodontal pockets. This instrument is essential during the initial assessment, allowing for the determination of the level of attachment loss and tracking the progression of periodontal diseases over time. In implant and oral surgery, it can also be used to verify biological dimensions and soft tissue thickness. The use of this probe allows for precise documentation of the gingival status, thus facilitating the establishment of an appropriate treatment plan. It is exclusively reserved for professional use by qualified practitioners, in accordance with the instructions provided by Hu-Friedy.

What are the technical characteristics of the instrument?

This periodontal probe is distinguished by its precise millimeter graduations. The Goldman-Fox #23 model features specific markings according to the 10-9-8-7-5-3-2-1 sequence, allowing for direct and rapid reading of measured depths. It is equipped with a #6 type handle, offering a grip adapted to the requirements of meticulous clinical examinations. The thinness of the working tip is designed to penetrate the gingival sulcus without causing unnecessary tissue damage, while transmitting a precise tactile sensation to the clinician. Manufactured by Hu-Friedy Mfg. Co., LLC, this probe benefits from the brand's expertise in designing high-precision manual instruments for periodontics and oral surgery.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified health professionals. Specific contraindications are not detailed in the raw technical documentation, but the use of the instrument should be avoided if the patient presents extreme sensitivities or acute inflammations that do not allow for risk-free insertion. It is imperative to read the instructions for use carefully before any intervention. The practitioner must evaluate the patient's clinical condition to determine if periodontal exploration using a metallic probe is appropriate. Compliance with sterilization and asepsis protocols is mandatory between each patient to prevent any risk of cross-contamination.

What are the maintenance and handling precautions?

As a non-absorbable Class I instrument, the Goldman-Fox periodontal probe requires rigorous maintenance to maintain its measurement performance. After each use, the instrument must be cleaned, decontaminated, and sterilized in accordance with Hu-Friedy guidelines and current hygiene standards. Care must be taken not to alter the graduations during cleaning to ensure the accuracy of future measurements. Regular inspection of the probe tip is recommended to ensure the absence of bending or dullness that could distort clinical results. Handling must be performed with care to preserve the integrity of the instrument and ensure patient safety during exploration of the gingival sulcus.

Who is the manufacturer and what standards are respected?

La sonde parodontale Goldman-Fox #23 est fabriquée par Hu-Friedy Mfg. Co., LLC, basée à Chicago, USA. Ce dispositif médical est classé en Classe I selon la réglementation en vigueur. En tant que fabricant reconnu dans le secteur de la chirurgie orale, Hu-Friedy applique des normes de fabrication rigoureuses pour assurer la conformité de ses instruments. Le produit est destiné exclusivement aux professionnels de santé qualifiés. Bien qu'un marquage CE spécifique ne soit pas précisé dans les données source, l'instrument satisfait aux exigences réglementaires applicables aux dispositifs médicaux de sa classe. Le respect des indications et avertissements du fabricant, mentionnés sur l'étiquetage, est essentiel pour garantir une utilisation sûre et efficace en milieu clinique.

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