Veneer NashTaylor instrument #6 handle straight
The Instr Veneer NashTaylor manche #6 droit is a medical device manufactured by le fabricant.
- Compliance: Medical device Class I.
- Manufacturer: le fabricant.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Veneer NashTaylor straight #6 handle instrument?
The Veneer NashTaylor instrument from the Hu-Friedy brand is a specialized tool in the INSTRU category, designed for demanding practitioners in aesthetic dentistry. This model is distinguished by its straight-shaped #6 handle, offering ergonomics adapted to meticulous manipulations. Manufactured under the supervision of le fabricant, this instrument is intended for the management of aesthetic restorative materials. As a Class I medical device, it meets the basic regulatory requirements for use in dental practices. Its structure is designed to allow fluid application, making it a reliable dental veneer instrument for bonding and modeling procedures of composite materials.
What are the clinical indications?
The clinical indications for this NashTaylor instrument from the Hu-Friedy brand primarily concern restorative and aesthetic dentistry. It is used during the placement of direct or indirect restorations. In practice, it serves as a dental veneer spatula for the application, placement, and smoothing of thin composites. Its use is indicated for healthcare professionals involved in aesthetic rehabilitation protocols where precision of movement is crucial for the biological and visual integration of the restoration. It allows for working on contours and ensuring a perfect transition between the restorative material and the natural tooth structure, thus optimizing the final result for the patient.
What are the technical characteristics?
Technically, this instrument from the Hu-Friedy brand is characterized by its straight number 6 handle, a configuration that promotes direct force transmission and high tactile precision. Referenced under the INSTRU category, this device is produced by the manufacturer Hu-friedy, located in Chicago, USA. Its design is specifically oriented towards the manipulation of veneers, making it an efficient veneer placement instrument. Although specific material details are not provided, its Class I classification indicates that it is a reusable manual instrument after sterilization, compliant with le fabricant manufacturing standards for professional dental instrumentation.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed in the raw technical documentation, other than the mandatory compliance with sterilization and standard clinical use protocols. As with any manual instrument, inappropriate use or use by untrained personnel constitutes a de facto contraindication. It is essential to refer to the instructions for use before any manipulation to ensure patient safety and instrument longevity. Use must be limited to the procedures for which the instrument was designed, notably as a veneer placement instrument.
What are the precautions for use and maintenance?
As a non-resorbable Class I device, precautions for use are based on maintaining the physical integrity of the instrument. The practitioner must inspect the NashTaylor instrument before each use to detect any signs of wear or deformation. Cleaning and sterilization must scrupulously follow the directives of le fabricant (Hu-friedy) to avoid any cross-contamination. As a veneer composite instrument, it is crucial to carefully clean the tips after each resin application to prevent material hardening on the tool, which could compromise the precision of future interventions. Storage must be in a dry and clean environment, in accordance with the manufacturer's warnings.
Who is the manufacturer and what standards are respected?
The official manufacturer of this instrument is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device belongs to Class I according to current regulations. Although specific CE marking is not mentioned in the source data, the product is manufactured according to rigorous quality standards intended for the professional healthcare market. The Hu-Friedy brand guarantees that this instrument meets the requirements of the intended use for dental surgeons. It is imperative to read the instructions provided by the manufacturer carefully before any use to ensure compliance with safety standards and recommended procedures for this type of manual instrumentation.
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Specifications
| Manufacturer | Hu-Friedy |
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