Sonde pigtail n°2 handle n°31 - Hu-Friedy - Delynov

What is the Hu-Friedy Pigtail #2 probe with #31 handle?

The Pigtail #2 probe with #31 handle, designed by the manufacturer Hu-Friedy, is a manual diagnostic instrument used in oral surgery and periodontology. This device consists of a specific working part, named Pigtail #2, mounted on a #31 type handle. Its structure is designed to offer a precise tactile response during the exploration of dental surfaces and supporting tissues. As a Hu-Friedy brand instrument, it benefits from the expertise of a recognized manufacturer in the design of tools for healthcare professionals. This device is classified as a Class I instrument according to current regulations, guaranteeing its compliance for professional use in dental offices or hospital environments.

What are the clinical indications for this instrument?

The use of the Hu-Friedy Pigtail #2 probe is primarily indicated for periodontal and dental clinical examination. It allows practitioners to detect the presence of calcified deposits, such as subgingival calculus, and to explore surface irregularities in the enamel or cementum. Its shape is particularly suited for evaluating furcation areas and complex interproximal spaces where a standard straight probe might lack precision. In oral surgery, it aids in identifying caries and verifying the adaptation of marginal restorations. This Hu-Friedy instrument is a fundamental diagnostic tool for establishing a precise treatment plan in implantology or periodontics.

What are the technical characteristics of the #31 handle?

The Pigtail #2 probe is equipped with the #31 handle from Hu-Friedy. This handle was designed to ensure a stable grip and optimal control during fine exploration phases. The connection between the #31 handle and the Pigtail #2 working end allows for faithful transmission of vibrations, essential for the tactile detection of tissue or dental anomalies. Although composition specifics are not detailed in the raw technical data, the Hu-Friedy design meets Class I requirements for medical devices. The lightness and diameter of the #31 handle aim to reduce muscle fatigue for the practitioner during prolonged examinations or systematic diagnostic procedures in the clinic.

What are the contraindications for the use of this probe?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, there are no specific medical contraindications listed for the use of this diagnostic instrument, beyond the standard protocols related to manual instrumentation. However, like any Class I medical device, its use is strictly reserved for qualified healthcare professionals. It is imperative to read the instructions for use carefully before any handling. Use should be avoided if the instrument shows signs of degradation or if the integrity of the Pigtail #2 working part is compromised, in order to guarantee patient safety and the reliability of the clinical diagnosis.

What are the maintenance and use precautions?

The Hu-Friedy Pigtail #2 probe, being a non-absorbable instrument intended for diagnosis, requires a rigorous sterilization and cleaning protocol between each patient, in accordance with the directives of Hu-Friedy Mfg. Co., LLC. Professionals must ensure that the instrument is correctly decontaminated before each use. It is recommended to regularly check the sharpness or condition of the Pigtail tip to maintain maximum tactile sensitivity. As indicated in the manufacturer's warnings, this device is reserved exclusively for professional use. Careful handling is necessary to avoid any deformation of the working end, which could distort the results of the periodontal or dental exploration.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a historical and recognized player in the field of dental and surgical instrumentation. This product is listed under Class I of medical devices. Compliance with this regulatory class indicates that the device meets the safety and performance requirements defined for non-invasive or minimally invasive diagnostic instruments. Practitioners can refer to the manufacturer's instructions to ensure use compliant with public health standards. Traceability and manufacturing quality are ensured by the rigorous industrial processes implemented by Hu-Friedy in the United States.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.