Periodontal probe number 12 handle number 30 Qulix 3-6-9-12 - Hu-Friedy - Delynov
The Sonde parodontale #12 manche #30 Qulix 3-6-9-12 - Hu-Friedy is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.
- Compliance: Medical device Class I.
- Manufacturer: Hu-Friedy Mfg. Co., LLC.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the periodontal probe #12 handle #30 Qulix?
The periodontal probe #12, manufactured by Hu-Friedy Mfg. Co., LLC, is a manual diagnostic instrument used in periodontology and oral surgery. It consists of a thin working end and a #30 type handle. This device is specifically equipped with Qulix marking, a system of colored graduations that facilitates the reading of millimeter measurements during clinical examination. As a diagnostic instrument, it allows for the evaluation of the supporting tissues of the tooth. This product belongs to the category of manual diagnostic instruments and meets the manufacturing standards of the Hu-Friedy brand, recognized for the quality of its devices in the dental sector.
What are the clinical indications?
This probe is indicated for the systematic evaluation of periodontal health. It is used to measure the depth of the gingival sulcus or periodontal pockets, identify gingival recessions, and evaluate the attachment level. In implant surgery, it can be used to measure soft tissue thickness or site depth. The use of this Hu-Friedy instrument is essential during the diagnostic, treatment planning, and post-therapeutic re-evaluation phases. It allows for the detection of early signs of periodontitis or peri-implantitis by providing quantitative data on the state of periodontal and peri-implant tissues.
What are the technical characteristics?
The periodontal probe #12 is distinguished by its Qulix graduation system with markers located at 3mm, 6mm, 9mm, and 12mm. These markings are designed not to fade during repeated sterilization cycles, ensuring long-lasting readability. The #30 handle offers a specific grip adapted to the needs of practitioners. The thinness of the working end allows for delicate insertion into the sulcus without causing unnecessary trauma to the soft tissues, while transmitting precise tactile feedback upon contact with the base of the pocket or the alveolar crest. The overall design of the instrument by Hu-Friedy ensures corrosion resistance and longevity in compliance with the requirements for Class I medical devices.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not detailed beyond the intended use. However, the use of this instrument should be avoided in patients with a known hypersensitivity to the materials constituting the instrument, although the exact composition is not specified here. It is imperative not to use the instrument if it shows signs of deformation or damage on the working part, as this could distort clinical measurements or injure the gingival tissues. As with any manual instrument, inappropriate use or the application of excessive force is contraindicated to prevent any iatrogenic damage.
What are the maintenance and durability precautions?
As the periodontal probe #12 is a non-resorbable and reusable instrument, it requires a rigorous cleaning, disinfection, and sterilization protocol after each use. It is recommended to carefully read the Hu-Friedy manufacturer's instructions before any handling. Practitioners must regularly inspect the integrity of the Qulix graduations (3-6-9-12) to ensure diagnostic accuracy. Maintenance in accordance with the guidelines for Class I instruments ensures patient safety and tool longevity. The use of inappropriate cleaning solutions could alter the marking or the surface condition of the steel, thereby compromising the probe's measurement function.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is 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 according to current regulations. As a Class I device, it meets the safety and performance requirements defined for surgical and diagnostic instruments that are non-invasive or transiently invasive. The mention 'Reserved for healthcare professionals' emphasizes that its use requires appropriate clinical expertise. Practitioners are invited to consult the instructions for use to become aware of all warnings and reprocessing instructions provided by Hu-Friedy.
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Specifications
| Manufacturer | Hu-Friedy |
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