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Precision Slender Line Debagging Pliers - Hu-Friedy - Delynov

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The Pince à débaguer Slim Line - 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.

204.00 € 204.0 EUR 204.00 € Tax Included

204.00 € Tax Included

(0.00 € / Units)
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Instrument

What is the Slim Line debanding plier - Hu-Friedy - Delynov?

The Slim Line debanding plier, designed by the manufacturer Hu-Friedy, is a specialized manual instrument used in orthodontics and oral surgery. Its structure is characterized by a refined design, optimized for intervention in restricted spaces where a standard plier might lack maneuverability. This medical device is specifically developed for the removal of attachments. As a Hu-Friedy product, it benefits from the expertise of a recognized manufacturer in the field of dental instrumentation. Its design meets the requirements of healthcare professionals seeking a reliable tool for the final stages of orthodontic treatments.

What are the clinical indications for this instrument?

This orthodontic debanding plier is indicated for the removal of bands and accessories bonded to dental surfaces. Its use is primarily centered on the debanding phase, a crucial step where the practitioner must remove orthodontic devices without altering the underlying enamel. Thanks to its Slim Line profile, it is particularly suitable for patients presenting dental crowding or difficult-to-access areas. The instrument is exclusively reserved for healthcare professionals trained in oral surgery and orthodontic techniques, ensuring a safe application in compliance with current clinical protocols.

What are the technical characteristics of the slim debanding plier?

The Hu-Friedy slim debanding plier is distinguished by its refined tips that allow for precise insertion under the edges of the bands. Although specific materials are not detailed in the provided technical documentation, the instrument complies with the manufacturing standards of Hu-Friedy Mfg. Co., LLC. Its geometry is designed to transmit the necessary force for detaching the attachment while minimizing bulk in the mouth. It belongs to the GBR (Guided Bone Regeneration) category within the Delynov catalog, although its primary function is related to the removal of orthodontic appliances.

What are the contraindications for the use of this device?

According to information from the manufacturer Hu-Friedy, specific contraindications are not listed exhaustively beyond general usage warnings. However, the use of this instrument is strictly reserved for qualified healthcare professionals. Use by an untrained person constitutes a major contraindication. It is imperative to read the instructions accompanying the product carefully before any clinical handling. The practitioner must assess the state of the dental and periodontal tissues before the intervention to ensure that the mechanical removal of the bands with this plier is appropriate for the patient's clinical situation.

What are the precautions for use for this non-resorbable instrument?

As it is a reusable metallic instrument and not a resorbable device like a suture, precautions mainly concern maintenance and handling. The Slim Line debanding plier must be cleaned, disinfected, and sterilized according to the protocols in force in dental surgery practices before each use. The practitioner must take care not to exert excessive pressure that could damage the instrument or dental structures. Hu-Friedy recommends scrupulously following the maintenance instructions provided by the manufacturer to guarantee the longevity and functionality of the plier during repeated debanding procedures.

Who is the manufacturer and what standards are respected?

The plier is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as a Class I instrument, in accordance with current regulations on medical devices. Compliance with this classification ensures that the product meets the safety and performance requirements defined for surgical instruments in this category. As a distributor, Delynov ensures that the information transmitted by Hu-Friedy is accessible to practitioners for use in accordance with the American manufacturer's guidelines.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

Specifications

Manufacturer Hu-Friedy
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