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Instrument composite no. 8A with handle no. 6 for anterior teeth - Hu-Friedy - Delynov

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The Instrument à composite #8A manche #6 antérieur - 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.

52.80 € 52.8 EUR 52.80 € Tax Included

52.80 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy anterior composite instrument #8A handle #6?

The composite instrument #8A with #6 handle is a specialized manual tool designed by the manufacturer Hu-Friedy for restorative dentistry procedures. This device consists of a working part specific to the anterior region and a #6 type handle, offering a grip adapted to the requirements of conservative surgery. As a composite shaper, it facilitates the application and sculpting of restorative materials. This product is manufactured by Hu-Friedy Mfg. Co., LLC, a recognized player in the design of high-precision instruments for healthcare professionals.

What are the clinical indications for this instrument?

This instrument is primarily indicated for aesthetic restorations in the anterior sector. It is used during the placement of composite resins to reconstruct dental morphology after caries removal or during aesthetic corrections. Its design is optimized for modeling the facial and lingual surfaces of incisors and canines. It allows the practitioner to manipulate the composite with precision before polymerization, thus ensuring optimal marginal adaptation and a reduction in rotary finishing time. Its use is strictly reserved for qualified healthcare professionals.

What are the technical characteristics of this instrument?

The Hu-Friedy instrument #8A is distinguished by its #6 handle, a standardized dimension from the manufacturer that promotes tactile control during restorative procedures. The active part is specifically sized for the cavities and surfaces of anterior teeth. Although material details are not specified in the MDR technical data, the overall design meets Class I medical device requirements. The geometry of the working end allows for smoothing and sculpting the composite without sticking to the material, thus facilitating the creation of natural anatomical contours.

What are the contraindications for the use of this instrument?

Specific contraindications mentioned by the manufacturer Hu-Friedy concern the intended use and compliance with safety warnings. There are no absolute medical contraindications listed outside of standard sterilization protocols and the handling of metal instruments in the oral environment. However, the use of this instrument must be avoided for any application other than that for which it was designed, notably the manipulation of materials not compatible with classic modeling instruments or excessive forces that could damage the active part.

What are the precautions for use and maintenance?

Like any Class I instrument intended for clinical practice, the Hu-Friedy composite shaper requires rigorous maintenance. The manufacturer Hu-Friedy Mfg. Co., LLC recommends reading the instructions carefully before use. Precautions include thorough cleaning followed by appropriate sterilization between each patient to prevent cross-contamination. It is imperative to check the integrity of the instrument before each use. Although this device is not resorbable (being a manual instrument and not an implant), its longevity depends on compliance with the decontamination cycles recommended by the manufacturer.

Who is the manufacturer and what standards are met?

The instrument is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, IL 60618 USA. This medical device belongs to Class I according to current regulations. The manufacturer ensures the compliance of its products with the quality standards required for surgical and restorative instruments. Professionals must refer to the instructions provided by Hu-Friedy to guarantee safe use in accordance with the manufacturer's indications. The CE marking is not specified in the technical documentation provided for this specific reference, but the product follows the classification directives for Class I medical devices.


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Specifications

Manufacturer Hu-Friedy
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