Williams Periodontal Probe #23 handle #31 10-9....3-2-1 thin

What is the Williams #23 periodontal probe with #31 handle?

The Williams #23 periodontal probe, offered by the brand Hu-Friedy, is a manual diagnostic instrument designed for the exploration of supporting tissues. It consists of a graduated working part and a handle referenced as #31. Its structure is specifically adapted for the millimeter measurement of subgingival spaces. This Class I medical device is manufactured by a recognized industry player, Hu-friedy, ensuring compliance with the manufacturing standards required for manual instrumentation. Its fine configuration allows for delicate insertion into the sulcus or periodontal pocket to obtain reliable clinical data during the initial assessment or post-operative follow-up.

What are the clinical indications for this instrument?

The use of the Williams probe from the brand Hu-Friedy is indicated for the quantitative evaluation of periodontal health. It allows the clinician to measure probing depth, identify the position of the cemento-enamel junction, and evaluate the extent of gingival recession. In implant surgery, it helps verify soft tissue thickness and the stability of peri-implant bone levels. The instrument is essential for establishing an accurate diagnosis of periodontitis and for monitoring the effectiveness of non-surgical or surgical treatments. Its use is strictly reserved for qualified healthcare professionals operating in a clinical environment.

What are the technical characteristics of the Williams probe?

This probe is distinguished by its specific Williams-type graduation, featuring markings at 1, 2, 3, 5, 7, 8, 9, and 10 mm. This sequence, which intentionally omits the 4 and 6 mm graduations, facilitates rapid reading and reduces interpretation errors during clinical measurements. The #31 handle is designed to provide a stable grip during the examination. The working part is extremely fine to minimize discomfort when passing through narrow or inflammatory areas. As a Hu-Friedy product, this instrument meets the precision requirements necessary for complex periodontal charting and routine interventions.

What are the contraindications for the use of this device?

According to data from the manufacturer Hu-friedy, the use of this instrument is reserved exclusively for trained healthcare professionals. There are no absolute medical contraindications listed in the provided technical documentation, other than standard protocols of caution related to acute inflammatory states of the gingival tissues which could skew measurements or cause excessive discomfort. It is imperative to read the instructions carefully before use to comply with safety guidelines. The practitioner must ensure that the patient's general health status does not present any particular risk during the clinical periodontal examination.

What are the maintenance precautions for this non-absorbable instrument?

As a reusable Class I metallic instrument, the Williams probe must undergo a rigorous sterilization protocol between each patient. Although specific material details are not provided, this type of manual instrumentation requires pre-disinfection cleaning followed by autoclave sterilization according to the standard cycles recommended by the manufacturer Hu-friedy. The integrity of the millimeter graduations should be inspected regularly to ensure measurement accuracy. Any instrument showing signs of wear, corrosion, or tip deformation must be removed from service to maintain the safety of care.

Who is the manufacturer and what standards are met?

The official manufacturer of this periodontal probe is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This device is classified as a Class I instrument according to current medical device regulations. Compliance with regulatory requirements ensures that the instrument is suitable for its intended use in surgical and dental environments. The brand Hu-Friedy distributes this product while ensuring compliance with the manufacturer's warnings. Professionals must systematically refer to the instructions for use and indications provided by Hu-friedy to ensure use in accordance with safety and clinical efficacy standards.

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