Periodontal Probe Novatech Number NT2 with Handle Number 6 Qulix 3-6-9-12 - Hu-Friedy - Delynov

What is the Novatech #NT2 handle #6 Qulix 3-6-9-12 perio probe?

The Novatech #NT2 perio probe is a periodontal diagnostic instrument designed by the manufacturer Hu-Friedy. It is characterized by a specific Novatech configuration and a #6 type handle. This instrument integrates the Qulix marking system, which features color-coded graduations at 3mm, 6mm, 9mm, and 12mm intervals. This device is essential for practitioners wishing to obtain precise measurements of the sulcus depth or periodontal pockets. Manufactured by Hu-Friedy Mfg. Co., LLC, this probe meets the quality requirements for manual instruments used in periodontology and oral surgery for the evaluation of supporting tissue health.

What are the clinical indications for this instrument?

This qulix perio probe is indicated for various diagnostic and monitoring procedures in periodontics. Its primary use lies in measuring the depth of periodontal pockets, thus allowing for the diagnosis of the extent of periodontal diseases. It is also used to evaluate the clinical attachment level, measure the height of keratinized gingiva, or quantify gingival recessions. In implantology, it can be used to measure the depth of peri-implant tissues. Its Novatech geometry is particularly suited for reaching posterior sectors with optimal angulation, facilitating the clinician's work during comprehensive examinations.

What are the technical characteristics of the Novatech #NT2 probe?

The technical characteristics of this Hu-Friedy instrument include a number 6 handle, recognized for its diameter promoting controlled grip. The working end features Qulix marking with clear visual cues at 3-6-9-12 mm, ensuring immediate reading and reducing parallax errors during probing. The Novatech design is distinguished by a specific shank angulation, allowing for easier vertical insertion in difficult-to-access areas, such as the distal surfaces of molars. As a Class I instrument, it is designed for repeated use after sterilization, respecting the rigorous manufacturing standards of Hu-Friedy Mfg. Co., LLC.

What are the contraindications for the use of this probe?

In accordance with the information from the manufacturer Hu-Friedy, the use of this instrument is reserved exclusively for qualified healthcare professionals. There are no specific medical contraindications listed outside of standard hygiene and sterilization protocols. However, use of the probe should be avoided on extremely inflammatory or friable tissues if excessive pressure is applied, to avoid causing trauma or false depth diagnoses. It is imperative to read the instructions carefully before use and to ensure that the instrument is correctly sterilized to avoid any cross-contamination between patients.

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

As it is a manual metallic instrument and not a resorbable device, the durability of the Novatech #NT2 probe depends on compliance with cleaning and sterilization cycles. After each use in surgery or clinical examination, the probe must be decontaminated, cleaned of all organic debris, and then sterilized according to the recommendations of the manufacturer Hu-Friedy. The integrity of the Qulix 3-6-9-12 markings should be checked regularly to ensure that measurement readings remain accurate. Careful handling is necessary to avoid bending the fine tip of the probe, which would distort clinical results during pocket probing.

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. As a recognized manufacturer in the dental sector, Hu-Friedy ensures production compliant with quality standards for surgical and diagnostic instruments. Although specific CE marking is not detailed in the source data, the product follows regulatory indications for Class I devices intended for healthcare professionals. Every user must imperatively consult the provided instructions for use to guarantee practice in accordance with the manufacturer's guidelines.

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