Periodontal Probe No. 10 with Handle No. 7 Qulix 1-2-3-5-7-8-9-10 - Hu-Friedy - Delynov

What is the Hu-Friedy #10 periodontal probe handle #7 Qulix?

The #10 periodontal probe is a precision diagnostic instrument manufactured by Hu-Friedy Mfg. Co., LLC. This model is distinguished by its handle #7 and its specific Qulix graduations (1-2-3-5-7-8-9-10). Designed for periodontal examination, it allows the practitioner to accurately measure the depth of the gingival sulcus or periodontal pockets. Qulix technology uses dark markings that contrast sharply with the brightness of the instrument, facilitating reading in humid clinical environments or under intense operating light. This instrument belongs to the INSTRU category and benefits from Hu-Friedy's historical expertise in designing manual tools for periodontology.

What are the clinical indications for this periodontal examination probe?

The use of this 10mm periodontal probe is indicated during all phases of periodontal diagnosis. It is used for measuring probing depth (PD), determining clinical attachment loss, as well as evaluating bleeding on probing. In oral surgery and implantology, it also serves to measure soft tissue thickness or to check the depth of implant sites. Its configuration with graduations up to 10mm covers the majority of clinical situations encountered during a complete periodontal examination, offering essential versatility for monitoring patients with periodontitis or gingivitis.

What are the technical characteristics of this Hu-Friedy instrument?

This 10 periodontal probe is characterized by a type #7 handle, offering a specific grip adapted to precision movements. The working part features millimeter graduations according to the Qulix sequence: 1, 2, 3, 5, 7, 8, 9, and 10mm. The absence of markings at the 4 and 6mm levels is a specific feature of the #10 probe, allowing for rapid identification of certain clinical thresholds. Manufactured by Hu-Friedy, the probe is designed to withstand repeated sterilization cycles while maintaining the sharpness of its markings. Its thinness allows for delicate insertion into the sulcus without damaging the epithelial attachment, thus ensuring a reliable and reproducible diagnosis.

What are the contraindications for the use of the periodontal diagnostic probe?

According to information from the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is reserved exclusively for qualified healthcare professionals. There are no absolute medical contraindications listed in the technical documentation; however, use must comply with the intended purpose of the device. Excessive pressure during probing must be avoided to prevent soft tissue trauma or false measurements due to attachment perforation. The practitioner must read the instructions carefully before use and ensure the integrity of the instrument before each clinical act to guarantee patient safety.

What are the maintenance precautions for this 10mm periodontal probe?

As a non-resorbable and reusable instrument, this periodontal probe requires a rigorous decontamination and sterilization protocol after each use. Although cleaning specificities are not detailed in the source text, it is standard practice in dental surgery to follow Hu-Friedy manufacturer recommendations to preserve the visibility of Qulix markings. Practitioners must ensure that all organic residue is removed before autoclaving. The durability of the probe depends directly on compliance with sterilization cycles and the absence of corrosive chemical products that could alter the precision of the millimeter graduations or the surface condition of the steel.

Who is the manufacturer and what standards are met by this device?

The #10 periodontal probe is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered in Chicago, USA. This medical device is classified as Class I according to current regulations. As a Class I product, it meets the safety and performance requirements defined for manual diagnostic instruments in dentistry. Mention of the manufacturer Hu-Friedy ensures traceability and compliance with industrial manufacturing standards for medical devices. It is reiterated that this instrument is strictly reserved for healthcare professionals and that consulting the instructions for use is mandatory to ensure use in accordance with safety standards.

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