Michigan Periosteal Probe Handle Number 6 3-6-8 - Hu-Friedy

What is the Michigan periodontal probe handle #6 3-6-8?

The Michigan periodontal probe is a manual diagnostic instrument designed by the manufacturer Hu-Friedy. It consists of a thin shank ending in a graduated working tip and a #6 type handle. This device is specifically calibrated with marking rings located at 3mm, 6mm, and 8mm. Its structure allows for fine exploration of the gingival sulcus. As an examination instrument, it facilitates the collection of clinical data essential for establishing a complete periodontal assessment. Hu-Friedy's manufacturing quality ensures consistency in graduations for constant reliability during repeated measurements in the practice.

What are the clinical indications for this instrument?

This Michigan probe is indicated for systematic periodontal examination. It allows practitioners to measure periodontal pocket depth, identify gingival recessions, and evaluate tissue hypertrophy. In implant surgery, it is used to monitor the stability of peri-implant tissues. The use of the periodontal examination probe is also required for screening the presence of subgingival calculus or root surface irregularities. The 3-6-8 graduations provide clear visual landmarks to quickly identify stages of periodontal disease and monitor the progress of non-surgical or surgical treatments.

What are the technical characteristics of the Hu-Friedy probe?

The Hu-Friedy Michigan periodontal probe is distinguished by its precise millimeter markings at 3, 6, and 8 mm. These graduations are obtained by a process guaranteeing their readability and resistance to sterilization cycles. The #6 handle features a specific diameter that improves tactile control when passing through difficult-to-access areas, such as the distal surfaces of molars. The thinness of the working part is designed to penetrate the sulcus with minimal resistance, allowing a faithful evaluation of the epithelial attachment. The instrument is designed to meet the requirements of daily practice in periodontology and restorative dentistry.

What are the contraindications for using this probe?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is reserved exclusively for qualified healthcare professionals. There are no specific medical contraindications listed in the technical documentation, apart from clinical situations where the state of the soft tissues or an acute infection would prohibit any instrumental manipulation. It is imperative to read the instructions for use carefully before any intervention. The practitioner must ensure the integrity of the instrument before use to avoid any risk related to a deformation of the tip or wear of the graduations which would distort the diagnosis.

What are the maintenance and handling precautions?

Although this product is classified as a non-resorbable instrument, its durability depends on compliance with cleaning and sterilization protocols. As a Class I device, it must be processed in accordance with Hu-Friedy guidelines to maintain the accuracy of the 3-6-8 markings. Particular attention must be paid to the removal of biological debris after each clinical examination. It is recommended to avoid the use of corrosive chemicals that could alter the steel surface or the visibility of the measuring rings. Proper storage in examination trays protects the fine tip of the probe against mechanical shocks.

Who is the manufacturer and what standards are respected?

The probe is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered in Chicago, USA. This medical device belongs to Class I according to current regulations. The manufacturer is globally recognized for the high quality of its dental and surgical instruments. Compliance with manufacturing standards ensures that each Michigan periodontal probe produced offers dimensional precision consistent with clinical standards. As a Class I device, it meets the essential safety and performance requirements for manual diagnostic instruments. Practitioners must refer to the manufacturer's instructions to ensure use in accordance with public health standards.

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