Periodontal Probe Kit number 10, including 12 tips and 2 handles - Hu-Friedy - Delynov.

What is the Perioscreen Probe Kit #10?

The Perioscreen Probe Kit #10 is a set of periodontal diagnostic instruments manufactured by Hu-Friedy. This specific kit consists of 12 interchangeable tips and 2 ergonomic handles, offering a complete solution for the clinical evaluation of periodontal tissues. Designed by Hu-Friedy Mfg. Co., LLC, this device provides practitioners with reliable equipment for systematic screening of periodontal diseases. As a perioscreen probe, this tool is essential for measuring pocket depth, identifying gingival recessions, and evaluating clinical attachment during initial assessments or periodontal maintenance follow-ups.

What are the clinical indications for the dental probe kit?

The Perioscreen dental probe kit is indicated for performing complete periodontal assessments in oral surgery and general practice. Its primary use lies in the millimeter measurement of attachment loss and the detection of bleeding on probing, early signs of gingival inflammation. This periodontics probe kit is particularly useful during diagnostic phases to differentiate gingivitis from periodontitis. It also allows for monitoring pocket evolution after root planing treatment or debridement surgery. The use of this equipment is strictly reserved for qualified healthcare professionals, in accordance with Hu-Friedy manufacturer guidelines.

What are the technical characteristics of this kit?

The perioscreen probe kit is distinguished by its configuration including 12 measurement tips and 2 handles, allowing for efficient instrumentation rotation during sterilization procedures or between different patients. Manufactured by Hu-Friedy Mfg. Co., LLC, each element of the kit is designed to meet the precision requirements of modern periodontology. The probes feature clear graduations for immediate reading of probing depth. The handle design ensures optimal grip for the practitioner, facilitating access to different areas of the dental arch while maintaining the tactile sensitivity necessary to detect subgingival irregularities or tartar deposits.

What are the contraindications for using these probes?

According to information provided by Hu-Friedy, the use of this device is reserved exclusively for healthcare professionals. Although the raw MDR text does not list specific medical contraindications related to the patient's condition, it is imperative to refer to the instructions for use before any intervention. Standard periodontal precautions apply, notably the need to adapt the pressure exerted during probing to avoid any trauma to soft tissues or the epithelial attachment. The use of these instruments must be avoided if the integrity of the tip is compromised or if the sterilization process has not been rigorously followed.

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

As non-absorbable metallic instruments, the probes in the Hu-Friedy kit require a strict decontamination and sterilization protocol after each use. The practitioner must ensure to carefully clean the 12 tips and 2 handles to remove all organic debris before autoclaving. It is crucial to regularly check the condition of the perioscreen probe graduations to ensure the accuracy of clinical measurements. Any tip deformation or marked wear of the millimeter markings must lead to the replacement of the concerned tip in order to maintain the reliability of the periodontal diagnosis and patient safety during the examination.

Who is the manufacturer and what standards are met?

The Perioscreen Probe Kit #10 is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device, meeting the regulatory requirements of its category for manual dental instrumentation. Hu-Friedy is a recognized manufacturer in the dental sector for the quality of its diagnostic and surgical instruments. Healthcare professionals using this kit must read the instructions for use provided by the manufacturer carefully to ensure use in compliance with the safety and clinical efficacy standards expected for this type of Class I device.

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