Skip to Content

XTS/composite spatula #I handle #6S XTS Composite Packing Instrument

https://www.delynov.fr/web/image/product.template/168571/image_1920?unique=bdceb30

The Spatule XTS/composites #I manche #6S XTS Composite Packing Instrument 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.

65.70 € 65.7 EUR 65.70 € Tax Included

65.70 € Tax Included

(0.00 € / Units)
  • Manufacturer

This combination does not exist.

Instrument

What is the XTS/composites spatula #I handle #6S?

The XTS/composites spatula #I, developed under the brand Hu-Friedy, is a manual instrument specifically designed for the manipulation of composite materials. This model, identified under the handle reference #6S, belongs to the category of restorative instrument kits. Its design aims to optimize the work of synthetic resins without excessive adhesion, allowing for fluid modeling of occlusal and proximal surfaces. As a Class I medical device, this instrument meets the basic regulatory requirements for use in dental surgery practices, ensuring secure integration into the daily care protocol of practitioners.

What are the clinical indications?

This instrument from the brand Hu-Friedy is indicated for all direct restoration procedures requiring the application of composites. It is particularly used during cavity filling phases where a composite packing instrument is necessary to condense the material. In conservative and restorative surgery, it allows for sculpting the anatomical contours of anterior and posterior teeth. Its use is strictly reserved for qualified healthcare professionals operating within the framework of dental care, restorative dentistry, or aesthetic dentistry to ensure the durability of adhesive restorations.

What are the technical characteristics?

The XTS/composites spatula #I handle #6S is distinguished by its ergonomic configuration adapted to the requirements of the practitioner's hand. Although specific materials are not detailed, the XTS range from the brand Hu-Friedy is recognized for its anti-adherent properties facilitating the work of viscous composites. The instrument is classified as a Class I device according to current regulations. It is designed to withstand standard sterilization cycles in a clinical environment, in accordance with the instructions from the manufacturer Hu-friedy located in Chicago, USA. Its structure allows for precise tactile control during the packing and smoothing of restorative materials.

What are the contraindications for use?

According to information provided by the manufacturer Hu-friedy, there are no specific medical contraindications listed for this instrument, other than its exclusive use by trained healthcare professionals. However, as with any manual instrument made of steel or alloy, its use is contraindicated in patients with a known hypersensitivity to metallic components if these are in direct contact with tissues. Reference should systematically be made to the attached instructions for use before any intervention to verify the suitability of the instrument with the patient's clinical status and the intended procedure.

What are the maintenance and use precautions?

As a non-resorbable and reusable instrument, the XTS spatula requires a rigorous decontamination and sterilization protocol after each patient. Professionals must carefully read the instructions before use to comply with the cleaning parameters recommended by the manufacturer. The instrument must be inspected regularly to detect any signs of wear or degradation of the active surface, which could compromise the quality of the composite packing or alter the handling properties of the restorative material. Proper maintenance ensures patient safety and the longevity of this Class I tool.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-friedy, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is marketed under the brand Hu-Friedy and holds a regulatory classification of Class I. Although CE marking is not specified in the source documentation, the device is manufactured according to rigorous industrial standards intended for the professional medical market. It is imperative for users to follow the manufacturer's guidelines to ensure compliance with the intended use and respect for the health safety standards in force in their geographical area.


State of the art

Single-use sterile surgical kits significantly reduce intraoperative contamination.

Specifications

Manufacturer Hu-Friedy
Tags
Tags
Instrument