North-Carolina Periodontal Probe #TU17 handle #31 15-14-13....3-2-1

What is the North-Carolina #TU17 periodontal probe with #31 handle?

The North-Carolina #TU17 periodontal probe, offered by the Hu-Friedy, is a manual diagnostic instrument designed for the exploration of the periodontium. It consists of a working part graduated from 1 to 15 mm (15-14-13....3-2-1) and a #31 handle. This instrument is manufactured by the manufacturer to meet the requirements of rigorous clinical examinations. Its structure allows for delicate insertion into the gingival sulcus to assess the health of the supporting tissues. As a Hu-Friedy product, it is included in the INSTRU catalog for routine interventions or pre-surgical periodontal assessments.

What are the clinical indications for this instrument?

This Hu-Friedy probe is primarily indicated for the millimeter measurement of periodontal pocket depth, the evaluation of the clinical attachment level, and the detection of gingival recessions. It is used systematically during comprehensive periodontal assessments, monitoring of implant sites, and planning for regenerative surgeries. Its continuous graduation up to 15 mm allows the practitioner to obtain precise data on the extent of periodontal lesions. Its use is essential for establishing a reliable periodontal diagnosis and for the post-operative follow-up of initial or surgical therapies in oral surgery.

What are the technical characteristics of the North-Carolina #TU17 probe?

The North-Carolina #TU17 probe is distinguished by its thin and elongated working part, marked with graduations ranging from 1 to 15 mm without interruption (15-14-13-12-11-10-9-8-7-6-5-4-3-2-1). The #31 handle offers a grip adapted to the precision movements required in periodontology. This device belongs to the INSTRU category and is classified as a Class I medical device. The design by the manufacturer ensures optimal readability of the millimeter markings, essential for the clinical documentation of patient records. Its manufacturing complies with the quality standards necessary for manual instrumentation used in surgical and dental environments.

What are the contraindications for using this probe?

The use of the North-Carolina #TU17 periodontal probe should be avoided on gingival tissues presenting severe acute inflammation or necrosis, where even light pressure could cause unnecessary tissue damage before stabilization. Although the manufacturer does not list specific medical contraindications in the data provided, the use of this instrument is strictly reserved for qualified healthcare professionals. Inappropriate handling or excessive pressure during probing can lead to trauma to the epithelial attachment or soft tissues. The instructions for use should always be referred to before any clinical intervention.

What are the maintenance and storage precautions?

As a non-resorbable and reusable Class I instrument, the North-Carolina probe must undergo a strict cleaning, disinfection, and sterilization protocol after each use, in accordance with the manufacturer's instructions. It is imperative to check the integrity of the millimeter graduations before each use to ensure the accuracy of the measurements. Practitioners must take care not to alter the tip of the probe during the instrument processing cycle. Regular inspection of the surface condition of the #31 handle and the working part is recommended to maintain the diagnostic performance of the instrument within the dental office or clinic.

Who is the manufacturer and what standards are met?

The official manufacturer of this device is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is a Class I medical device, which implies compliance with basic regulatory requirements for manual surgical instruments. The probe is distributed under the Hu-Friedy and belongs to the INSTRU category. In accordance with medical device directives, the manufacturer specifies that the use of this instrument is exclusively reserved for healthcare professionals. Users are invited to read the instructions carefully before use to ensure compliance with safety and clinical efficacy protocols during periodontal diagnostic procedures.

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