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Periodontal Probe Number 2 Handle Number 6 Qulix 2-4-6-8-10-12 - Hu-Friedy - Delynov

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The Sonde parodontale #2 manche #6 Qulix 2-4-6-8-10-12 - 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.

46.20 € 46.2 EUR 46.20 € Tax Included

46.20 € Tax Included

(0.00 € / Units)
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Instrument

What is the periodontal probe #2 handle #6 Qulix?

The periodontal probe #2 from the Hu-Friedy brand is a manual diagnostic instrument designed for exploring the sulcus and periodontal pockets. This specific model is distinguished by its #6 handle, offering an optimized diameter for clinical handling, and its working end featuring Qulix marking. The periodontal probe n2 features precise graduations of 2, 4, 6, 8, 10, and 12 millimeters, applied by a durable black marking process that facilitates direct visual reading in the mouth. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets the quality standards of a recognized manufacturer in the field of surgical and dental instrumentation.

What are the clinical indications?

The periodontal probe cp2 is indicated for the systematic assessment of the health of the tooth's supporting tissues. In oral surgery and periodontology, it is used to measure pocket probing depth, identify the presence of bleeding on probing, and quantify clinical attachment loss. It is also employed to measure soft tissue dimensions before implant placement or to monitor the stability of peri-implant tissues during follow-up visits. Its design allows for fine exploration of the gingival sulcus to detect subgingival irregularities and guide the therapeutic or surgical treatment plan.

What are the technical characteristics of this probe?

This periodontal probe 2 is characterized by a working part calibrated according to the Qulix scale, with visual markers located at 2mm, 4mm, 6mm, 8mm, 10mm, and 12mm. The #6 type handle is designed to provide a balanced grip. The instrument is classified as a Class I device according to current regulations. The precision of the marking is essential to guarantee the reproducibility of measurements between different clinical examinations of the same patient. The finish of the tip is designed to allow smooth insertion into the sulcus, while transmitting the tactile information necessary for the practitioner to detect the bottom of the pocket or the presence of subgingival calculus.

What are the contraindications for use?

In accordance with the information from the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is reserved exclusively for qualified healthcare professionals. There are no specific medical contraindications listed in the provided technical documentation, outside of clinical situations where periodontal probing itself would be prohibited (for example, during certain acute phases of uncontrolled infections or on extremely fragile tissues requiring a different approach). It is imperative to read the instructions for use carefully and respect standard sterilization protocols before any intervention on a patient to avoid risks of cross-contamination.

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

As it is a non-absorbable metallic instrument, the Hu-Friedy #2 periodontal probe requires a complete cycle of cleaning, disinfection, and sterilization between each patient. Precautions for use include regular inspection of the working end to ensure that the Qulix graduations (2-4-6-8-10-12) remain perfectly legible and that the tip shows no deformation or excessive wear that could distort the millimeter measurements. Rigorous maintenance guarantees the longevity of the instrument and the safety of care. It is recommended to use cleaning solutions compatible with high-quality stainless steel instruments to preserve the integrity of the black marking.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, USA. This medical device belongs to Class I. As a Hu-Friedy product, it benefits from the expertise of a manufacturer recognized for its rigorous manufacturing processes. Although specific CE marking is not detailed in the source data, the product complies with the regulatory requirements applicable to Class I medical devices intended for healthcare professionals. Each user must refer to the technical notice and manufacturer's instructions to ensure use compliant with the safety and clinical efficacy standards expected in a dental office.


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Specifications

Manufacturer Hu-Friedy
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