Periodontal Probe Novatech Number NT12 Qulix 1-2-3-....-10-11-1 - Hu-Friedy
The Sonde paro Novatech #NT12 manche #6 Qulix 1-2-3-....-10-11-12 - 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 Hu-Friedy Novatech #NT12 periodontal probe?
The Novatech #NT12 periodontal probe, manufactured by Hu-Friedy, is a manual diagnostic instrument used in dentistry to evaluate the health of the tooth's supporting tissues. This model is distinguished by its #6 handle and its working end featuring Qulix marking, offering a series of graduations ranging from 1 to 12mm (1-2-3-4-5-6-7-8-9-10-11-12). Its structure is specifically designed to allow clear and precise reading of probing depths during clinical examinations. As a precision instrument, it assists the practitioner in establishing a reliable periodontal diagnosis, essential before any surgical or implant intervention.
What are the clinical indications for this instrument?
The use of the Hu-Friedy Novatech #NT12 probe is indicated for measuring periodontal pocket depth, evaluating attachment loss, and detecting bleeding on probing. In oral surgery and periodontology, it allows mapping of the patient's gingival status and monitoring tissue healing after scaling and root planing or resective surgery. Qulix graduations facilitate clinical documentation by providing consistent millimetric measurements. This instrument is indispensable for the regular monitoring of patients with periodontitis or for peri-implant maintenance to prevent inflammatory complications.
What are the technical characteristics of the Novatech #NT12 probe?
The Novatech #NT12 probe is characterized by its #6 type handle, designed by Hu-Friedy to offer handling stability during intra-oral measurements. Its fine tip is marked according to the Qulix system, which features alternating black bands for each millimeter from 1 to 12. This technical specificity guarantees excellent visibility, even in the presence of oral fluids or in difficult-to-access areas. Unlike probes with spaced graduations, the continuous 1-2-3-4-5-6-7-8-9-10-11-12 sequence allows for increased precision without visual extrapolation, thus securing the collection of clinical data for the patient file.
What are the contraindications for the use of this probe?
According to the information provided by 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 outside of standard asepsis and sharp instrument handling protocols. However, the practitioner must exercise caution when examining extremely inflammatory tissues or in the presence of fragile prosthetic restorations to avoid any iatrogenic trauma. It is imperative to read the instructions for use carefully before any clinical handling to ensure the safety of the patient and healthcare staff.
What are the maintenance precautions for this non-absorbable instrument?
As a metallic diagnostic instrument and not a resorbable device like a suture, the Hu-Friedy Novatech #NT12 probe requires a strict sterilization protocol between each patient. Although composition specificities are not detailed here, Hu-Friedy Class I instruments must be cleaned, disinfected, and sterilized in accordance with the manufacturer's instructions and current hygiene standards in the dental office. Particular attention must be paid to cleaning the Qulix graduations to maintain their legibility over the long term. Rigorous maintenance prevents corrosion and ensures the longevity of surgical instrumentation.
Who is the manufacturer and what standards are respected?
The Novatech #NT12 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. Hu-Friedy is a recognized manufacturer in the dental sector for the quality of its manual instrumentation. Compliance with Class I indicates that the product meets the safety and performance requirements for reusable surgical instruments. Practitioners should refer to the technical notice provided by Hu-Friedy to ensure compliance with use and reprocessing protocols in accordance with the regulatory directives applicable to medical devices.
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Specifications
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