North Carolina Periodontal Probe #23 handle #7 12-11-10....3-2-1

What is the North Carolina #23 periodontal probe with #7 handle?

The North Carolina #23 periodontal probe with #7 handle marketed by Hu-Friedy is a manual diagnostic instrument designed for periodontal exploration. This device is distinguished by its working part graduated from 1 to 12mm (12-11-10....3-2-1), allowing for precise millimeter reading of the biological space. It is equipped with a #7 type handle, offering a grip adapted to the requirements of diagnostic procedures in oral surgery. As a product of Hu-Friedy, this instrument meets the manufacturing standards of a recognized manufacturer in the field of dental instrumentation, guaranteeing reliability during daily clinical examinations.

What are the clinical indications?

The clinical indications for this Hu-Friedy instrument primarily concern the evaluation of periodontal health. It is used by healthcare professionals to measure the probing depth of periodontal pockets, identify attachment loss, and quantify gingival recessions. In implant surgery, this probe is useful for checking soft tissue thickness or the depth of implant sites. Its use is strictly reserved for qualified healthcare professionals, in accordance with the directives of the manufacturer Hu-friedy located in Chicago. The instrument allows for rigorous monitoring of periodontal pathologies and the planning of surgical or non-surgical interventions necessary to maintain tissue integrity.

What are the technical characteristics?

The North Carolina #23 periodontal probe is characterized by an exhaustive graduation ranging from 1mm to 12mm. Each millimeter is distinctly marked on the shank to ensure unambiguous reading of clinical measurements. The #7 handle is designed to ensure controlled handling during probing. This medical device belongs to Class I according to current regulations. It is manufactured by Hu-friedy, a manufacturer established in the USA. The design of the instrument aims to provide a precise tactile response during the exploration of the sulcus or periodontal pockets, thus facilitating the differential diagnosis between healthy gingiva and periodontitis.

What are the contraindications for use?

In accordance with the information provided by the manufacturer Hu-friedy for this Hu-Friedy product, specific contraindications are not detailed beyond the intended use. However, the use of this instrument is strictly reserved for healthcare professionals. Inappropriate use by unqualified personnel constitutes a major contraindication. It is imperative to read the instructions carefully before any use to ensure compliance with asepsis and handling protocols. As with any invasive diagnostic instrument, its use should be avoided on tissues presenting uncontrolled acute inflammation if the procedure risks further altering tissue integrity without immediate diagnostic benefit.

How is maintenance performed and what are the precautions?

As a non-resorbable Class I instrument, the North Carolina #23 periodontal probe requires a rigorous sterilization protocol between each patient. Although composition details are not specified, Hu-Friedy instruments must be cleaned, disinfected, and sterilized according to current hospital standards. It is crucial to check the integrity of the millimeter graduations before each use, as wear of the markings could distort clinical measurements. Precautions for use include delicate handling to avoid any trauma to the epithelial attachment during probing. Compliance with the instructions from manufacturer Hu-friedy is essential to guarantee the longevity and precision of the instrument.

Who is the manufacturer and what standards are respected?

The official manufacturer of this probe is Hu-friedy, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I, which corresponds to reusable surgical instruments presenting a low risk. Hu-Friedy ensures the distribution of this instrument intended exclusively for healthcare professionals. Although CE marking is not specified in the source data, the product is subject to strict regulations governing Class I medical devices. Practitioners must systematically refer to the instructions for use provided by the manufacturer to ensure practice compliant with safety and clinical performance requirements.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.