Periodontal probe number 12 with handle number 6 Qulix - Hu-Friedy - Delynov

What is the Hu-Friedy #12/QOW periodontal probe?

The #12/QOW periodontal probe with #6 Qulix handle, designed by Hu-Friedy, is a manual diagnostic instrument used in dentistry. It consists of a graduated working part and an ergonomic #6 type handle. This specific model incorporates Qulix marking technology, characterized by color-coded graduations that do not fade, thus facilitating direct visual reading during clinical examination. As a Class I medical device, this probe is a standard tool for evaluating the health of the tooth's supporting tissues. Its design by Hu-Friedy Mfg. Co., LLC guarantees an instrument that meets the requirements of practitioners for regular periodontal assessments.

What are the clinical indications for this instrument?

This qulix probe is primarily indicated for measuring the depth of the sulcus or periodontal pockets. It allows the clinician to quantify attachment loss, detect bleeding on probing, and identify the presence of subgingival calculus or root anatomical anomalies. Its use is systematic during diagnostic phases, treatment planning, and periodontal maintenance sessions. It is also useful for evaluating gingival recession and the width of keratinized gingiva. The instrument is exclusively reserved for healthcare professionals trained in periodontal probing techniques, ensuring precise and respectful handling of soft tissues.

What are the technical characteristics of the #12/QOW probe?

The #12/QOW periodontal probe is distinguished by its Qulix marking system, which offers optimal visibility of millimeter graduations. The #6 handle is designed to provide a stable grip, reducing hand fatigue during prolonged examinations. Manufactured by Hu-Friedy, this probe benefits from the manufacturer's own quality finish, ensuring a thin, rounded tip to minimize patient discomfort while maintaining sufficient rigidity for precise tactile transmission. Although the periodontal probe price may vary by distributor, this instrument is recognized for its longevity and resistance to repeated sterilization cycles in the dental office.

What are the contraindications for the use of this probe?

According to data from the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is reserved for qualified healthcare professionals. There are no specific medical contraindications listed in the provided technical documentation, other than the usual precautions related to acute inflammatory states of the gingival tissues which could distort measurements or cause excessive discomfort. It is imperative to read the instructions carefully before use to ensure compliance with asepsis and handling protocols. The instrument must not be used for functions other than the periodontal probing for which it was designed.

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

As a non-resorbable Class I metallic instrument, the #12/QOW periodontal probe requires a rigorous decontamination, cleaning, and sterilization protocol after each use. It is recommended to follow Hu-Friedy's specific guidelines to preserve the integrity of the Qulix markings and the handle. Practitioners should regularly inspect the probe tip for any deformation or wear of the graduations that could compromise the accuracy of clinical measurements. Proper maintenance ensures not only patient safety but also the longevity of the investment in this essential diagnostic instrument.

Who is the manufacturer and what standards are met?

The 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 Hu-Friedy product, it is designed according to strict manufacturing standards to meet the needs of dental surgeons and periodontists. The manufacturer emphasizes the importance of consulting the instructions for use attached to the product to ensure use in accordance with safety and efficacy standards. Although CE marking is not specified in the source data, the instrument meets the regulatory requirements applicable to medical devices of its class for professional marketing.

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