Periodontal Probe #23 handle #6 11-8-6-3

What is the Periodontal Probe #23 handle #6 11-8-6-3?

The Periodontal Probe #23 handle #6 11-8-6-3 marketed under the brand Hu-Friedy is a manual diagnostic instrument designed for the exploration of supporting tissues. This device consists of a graduated working part and a number 6 handle, offering a configuration adapted to rigorous clinical examinations. Its structure allows the practitioner to accurately assess the space between the gum and the tooth or implant. As a product of the brand Hu-Friedy, this instrument meets the needs of practices specializing in periodontology and oral surgery. Its design aims to provide a reliable tactile response during insertion into the sulcus, thus facilitating the collection of clinical data essential for periodontal diagnosis.

What are the clinical indications?

The clinical indications for this probe from the brand Hu-Friedy primarily include measuring the probing depth of periodontal and peri-implant pockets. It is used to detect loss of attachment, evaluate gingival recessions, and check for the presence of bleeding on probing. In implant surgery, it allows for monitoring the stability of peri-implant tissue health. The instrument is also indicated for exploring furcations and detecting subgingival irregularities. Its use is strictly reserved for qualified healthcare professionals, in accordance with the instructions from the manufacturer Hu-friedy, ensuring appropriate handling during diagnostic or post-operative follow-up procedures.

What are the technical characteristics?

The Periodontal Probe #23 is distinguished by its specific 11-8-6-3 graduations, which allow for a clear and rapid reading of measured depths in mm. The number 6 handle is designed to provide a grip adapted to the requirements of daily clinical practice. This medical device belongs to Class I, which corresponds to the regulatory standards for non-invasive or reusable surgical instruments in this category. The precision of the markings on the working part is essential to ensure the reproducibility of measurements between different examinations, a key factor for the longitudinal follow-up of patients with periodontal pathologies. Manufacturing is carried out by the manufacturer Hu-friedy, located in the USA.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-friedy, specific contraindications are not detailed beyond general warnings for use. However, the use of this instrument should be avoided in patients with a known hypersensitivity to the materials constituting the device, although the exact composition is not specified here. It is imperative not to use the instrument if it shows signs of degradation or illegible graduations, which could distort the clinical diagnosis. As specified in the technical documentation, use is exclusively reserved for trained healthcare professionals, and a careful reading of the instructions is required before any intervention to prevent any iatrogenic risk.

What are the maintenance and durability precautions?

As a Class I instrument intended for professional use, the Periodontal Probe #23 from the brand Hu-Friedy requires a rigorous sterilization and cleaning protocol between each patient. Although details on resorption do not apply to this non-resorbable metallic instrument, its durability depends on compliance with the decontamination cycles recommended by the manufacturer Hu-friedy. The integrity of the working tip and the legibility of the 11-8-6-3 graduations should be checked regularly. Improper maintenance could alter the precision of the millimeter measurements. Practitioners must systematically refer to the instructions for use to guarantee the longevity of the instrument and the safety of the care provided in a sterile environment.

Who is the manufacturer and what standards are respected?

The official manufacturer of this medical device is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device, thus respecting the regulatory requirements in force for this category of instruments. The mention of the manufacturer and their address guarantees the traceability of the product within the medical supply chain. In accordance with the Medical Device Regulation (MDR), this instrument is reserved exclusively for healthcare professionals. Although specific CE marking is not mentioned in the source data, membership in Class I indicates compliance with self-certification processes for manual diagnostic surgical instruments.

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