Periodontal probe number 12 handle number 6 Qulix 3-6-9-12 - Hu-Friedy - Delynov

What is the #12 periodontal probe #6 Qulix handle?

The #12 periodontal probe designed by Hu-Friedy is a manual diagnostic instrument used in periodontology. It consists of a thin, calibrated working part mounted on a large diameter #6 handle. This device incorporates the Qulix marking system, characterized by high-precision colored graduations. Unlike treatment instruments, this probe is a measurement unit intended for the clinical exploration of the soft tissues surrounding the tooth. Its structure is optimized to transmit tactile sensations to the practitioner when exploring the sulcus or periodontal pockets, thus facilitating a rigorous diagnosis.

What are the clinical indications for this instrument?

This instrument is indicated for performing a complete periodontal chart. It allows for the precise measurement of attachment loss in millimeters, quantification of gingival recessions, and verification of the presence of bleeding on probing. In implant surgery, it can be used to evaluate the height of peri-implant tissues. The #12 probe is particularly suitable for routine examinations and post-operative follow-ups thanks to its markings spaced 3 mm apart. Its use is strictly reserved for healthcare professionals qualified in oral and dental surgery for the evaluation of patients' periodontal health.

What are the technical characteristics of the #12 Qulix probe?

The Hu-Friedy #12 periodontal probe is distinguished by its Qulix marking system, featuring visual segments at 3, 6, 9, and 12 mm levels. These graduations are applied with extreme precision to avoid parallax reading errors. The #6 handle is a large diameter satin steel handle, offering a specific configuration for manual gripping. The tip is calibrated to be thin enough to penetrate the sulcus without excessive trauma, while maintaining the necessary rigidity for a reliable measurement. The overall design of the instrument meets the requirements for durability and resistance to repeated sterilization cycles in the dental office.

What are the contraindications for using this probe?

There are no absolute medical contraindications listed by the manufacturer Hu-Friedy Mfg. Co., LLC for the use of this measuring instrument, outside of clinical situations where periodontal probing is temporarily prohibited (for example, during certain acute phases of uncontrolled infections or on extremely fragile tissues requiring primary healing without manipulation). However, the practitioner must refer to the instructions before use to become aware of specific warnings. The instrument must not be used for leverage or curettage functions, as this could damage the calibrated tip or injure the patient's tissues.

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

As a Class I non-absorbable metallic instrument, the probe must be subject to a strict decontamination and sterilization protocol between each patient. It is imperative to carefully clean the Qulix graduations to maintain optimal visibility of the 3-6-9-12 measurements. Biological residues can alter the accuracy of the reading and compromise asepsis. It is recommended to use neutral pH cleaning solutions to preserve the integrity of the marking and the steel. Regular inspection of the tip is necessary to ensure it is neither bent nor dull, which would distort the periodontal diagnostic results.

Who is the manufacturer and what standards are respected?

The #12 periodontal probe is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. As a globally recognized manufacturer in the dental instrumentation sector, Hu-Friedy guarantees that this instrument meets the safety and performance requirements for professional medical devices. Practitioners must carefully read the instructions for use provided by Hu-Friedy before any intervention. Compliance with cleaning and sterilization protocols is essential to ensure the continued conformity of the instrument to clinical hygiene standards.

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