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NSK G1 Implant (Z217101) - Delynov

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The Insert G1 NSK is a medical device manufactured by NSK Dental.

  • Manufacturer: NSK Dental.
  • Reference: Z217101.
  • Reserved for healthcare professionals. Read instructions carefully before use.

98.20 € 98.2 EUR 98.20 € Tax Included 138.61 €

98.20 € Tax Included 138.61 €

(98.20 € / Units)
  • Manufacturer

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Equipment

What is the NSK G1 Tip (Z217101) - Delynov?

The NSK G1 tip is a dental ultrasonic instrument specifically developed for prophylaxis interventions. Identified under the technical reference Z217101, this device is part of the range of consumables for ultrasound generators from the NSK brand. Its design is optimized for the treatment of dental surfaces, offering practitioners a precision tool for routine hygiene care. As part of the CONSO category at Delynov, it meets the requirements for periodontal maintenance in a clinical setting, ensuring a reliable interface between the ultrasonic equipment and the patient.

What are the clinical indications for this NSK scaler tip?

The NSK G1 tip is primarily indicated for supra-gingival scaling. In oral surgery and periodontology, its use is recommended for the removal of calcified tartar deposits located above the gum line. It is used during professional cleaning sessions to sanitize the oral cavity before more complex interventions or as part of regular follow-up. This dental ultrasonic tip effectively treats interdental spaces and smooth surfaces, thus contributing to the prevention of periodontal diseases and the preparation of the surgical field.

What are the technical characteristics of the NSK G1 tip?

The NSK G1 tip is distinguished by its catalog reference Z217101. It is a G1 type tip, a standardized geometry recognized for its versatility during initial scaling phases. Although detailed material specifications are not explicitly listed, this type of ultrasonic tip is designed to transmit the high-frequency vibrations necessary for the disintegration of tartar. Its connection is strictly compatible with ultrasonic handpieces from the manufacturer NSK Dental, guaranteeing stable energy transmission and optimal irrigation throughout the clinical procedure.

What are the contraindications for the use of this scaling tip?

The contraindications for the use of the NSK G1 tip are those generally associated with the use of ultrasounds in dental medicine. Although the source document does not specify contraindications specific to this Z217101 model, caution is advised in patients with active implantable medical devices, such as pacemakers, unless otherwise indicated by the device manufacturer. Furthermore, use on soft tissues or exposed root surfaces without precaution can lead to sensitivity. It is imperative to systematically refer to the instructions for use provided by NSK Dental to validate the absence of specific restrictions.

What precautions for use and maintenance are necessary?

To guarantee the longevity of the NSK G1 tip and the safety of care, several precautions must be observed. Like any NSK scaling tip, tip wear must be checked regularly; a loss of length can reduce vibration efficiency and increase the necessary pressure, which is counterproductive. The practitioner must ensure sufficient irrigation to avoid any thermal heating of the dental tissues. The cleaning, disinfection, and sterilization protocol must strictly follow the recommendations of the manufacturer NSK Dental to prevent cross-contamination and maintain the structural integrity of reference Z217101.

Who is the manufacturer of the Z217101 tip and what are the standards?

The NSK G1 tip is manufactured by NSK Dental, a globally recognized player in the design of rotary and ultrasonic devices for dentistry. Manufacturing by NSK Dental ensures perfect compatibility with their proprietary ultrasonic systems. Regarding specific certifications such as the regulatory class or CE marking, this information is not detailed in the current source data. Professionals are invited to consult the product labeling and the manufacturer's official technical documentation to confirm compliance with current European standards before any clinical implementation.


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