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Excavator number 31L handle number 41 pulpal - Hu-Friedy - Delynov

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The Excavateur #31L manche #41 pulpaire - 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.

61.95 € 61.95 EUR 61.95 € Tax Included

61.95 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy #31L pulp excavator with #41 handle?

The #31L excavator with #41 handle is a specialized manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. It belongs to the category of endodontic and surgical instruments. This device is specifically structured for intervention at the level of the pulp chamber. Its configuration with the #41 handle offers a grip adapted to the requirements of precise clinical movements. As a Hu-Friedy brand instrument, it benefits from the expertise of a recognized manufacturer in the field of dental instrumentation, guaranteeing manufacturing quality compliant with professional standards for pulp interventions.

What are the clinical indications for this pulp excavator?

This pulp excavator is primarily indicated for endodontic procedures. It is used by dental surgeons for the evacuation of dental pulp, whether healthy, inflamed, or necrotic, during a pulpotomy or the start of a root canal treatment. Its role is crucial for the mechanical cleaning of the pulp chamber and the elimination of deep or softened carious dentin. It also allows for the removal of temporary filling materials or calcified debris that could obstruct access to the root canals, thereby facilitating the subsequent steps of canal preparation.

What are the technical characteristics of this instrument?

The #31L excavator is distinguished by the geometry of its working part, optimized for pulp curettage. Associated with the Hu-Friedy #41 handle, the assembly is designed to offer adequate balance during intra-oral manipulations. Although exact material specifications are not detailed in the source data, Hu-Friedy instruments are recognized for their resistance to repeated sterilization cycles. This device is classified as a Class I instrument according to current regulations, which corresponds to medical devices presenting a low degree of risk, suitable for professional use in dental offices or hospital environments.

What are the contraindications for the use of this excavator?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, there are no specific medical contraindications listed for this instrument, other than general contraindications related to dental surgery or endodontic procedures. Use must be strictly limited to the intended indications. The practitioner must evaluate the patient's clinical condition and ensure that the instrument is used in accordance with its intended purpose. As indicated in the regulatory text, this device is reserved exclusively for qualified healthcare professionals with in-depth knowledge of endodontic care protocols.

What are the precautions for use and maintenance?

As a non-resorbable and reusable instrument, this pulp excavator requires a rigorous decontamination and sterilization protocol between each patient. Before the first use and after each procedure, it is imperative to carefully read the instructions provided by the manufacturer. Precautions include visual inspection of the instrument to detect any signs of wear or corrosion on the #31L working part or the #41 handle. Inappropriate maintenance could compromise the effectiveness of the curettage or the longevity of the tool. Compliance with the sterilization parameters recommended by Hu-Friedy is essential to guarantee the safety of the patient and the healthcare staff.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered in Chicago, USA. This product is a Class I medical device. Manufacturing by Hu-Friedy guarantees compliance with the strict quality standards associated with surgical instruments. Although specific CE marking is not mentioned in the source data, the product complies with the regulatory requirements applicable to devices of its class for professional marketing. It is reminded that the use of this excavator is strictly reserved for healthcare professionals and that reading the instructions is mandatory before any clinical manipulation.


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Manufacturer Hu-Friedy
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