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Adson Brown Tissue Forceps Number 43 Surgery 7x7 Straight 12cm - Hu-Friedy - Delynov

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The Pince à tissus Adson Brown #43 chirug. 7x7-droite 12cm - 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.

74.10 € 74.1 EUR 74.10 € Tax Included

74.10 € Tax Included

(0.00 € / Units)
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Instrument

What is the Hu-Friedy adson brown #43 forceps?

The adson brown #43 forceps is a precision surgical instrument developed by Hu-Friedy, a recognized manufacturer in the dental sector. This device is distinguished by its specific 7x7 teeth configuration, designed to ensure a firm but controlled grip of soft tissues. Its straight structure and 12cm length make it a tool particularly suited to the restricted spaces of the oral cavity. As an instrument in the GBR (Guided Bone Regeneration) category, it allows practitioners to handle flaps with great stability, thus limiting the risk of slipping during critical phases of the surgical intervention.

What are the clinical indications for this instrument?

This adson brown forceps is primarily indicated for oral surgery, periodontology, and implantology procedures. It is used to grasp and hold soft tissues, such as gums or mucosa, during the exposure of the surgical site or during the placement of sutures. Its use is also relevant during guided bone regeneration protocols for the manipulation of membranes and the stabilization of surrounding tissues. The instrument is strictly reserved for healthcare professionals trained in surgical techniques, guaranteeing use in accordance with the clinical requirements of Hu-Friedy Mfg. Co., LLC.

What are the technical characteristics of the forceps?

The Adson Brown #43 tissue forceps features precise technical specifications to meet the needs of surgeons. It has a total length of 12cm, offering an optimal balance between maneuverability and clinical access. The working part is equipped with 7x7 straight teeth, an essential feature for effective tissue grip without excessive trauma. Manufactured by Hu-Friedy, this forceps benefits from the industrial expertise of the Chicago-based manufacturer. It belongs to Class I of medical devices, which regulates its use in a strict professional surgical environment.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not detailed beyond standard usage warnings. However, the use of this instrument is strictly reserved for qualified healthcare professionals. It is imperative not to use the instrument for tasks for which it is not intended, such as the manipulation of rigid materials that could damage the 7x7 teeth. The practitioner must systematically refer to the instructions for use before any intervention to ensure the suitability of the tool for the pathology being treated.

What are the maintenance precautions for this non-resorbable forceps?

As a non-resorbable metallic surgical instrument, the adson brown forceps requires a rigorous sterilization and cleaning protocol after each use. Although composition details are not specified, Hu-Friedy instruments are designed to withstand standard disinfection and autoclave cycles specific to dental practices. It is crucial to check the integrity of the 7x7 teeth before each use to guarantee optimal grip. Compliance with the instructions from the manufacturer Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA is essential to maintain the longevity and safety of this Class I device.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. As a Hu-Friedy product, it meets the manufacturing standards of a major player in global surgical instrumentation. Compliance with regulatory requirements ensures that the instrument is suitable for professional use in a clinical setting. Practitioners are invited to carefully read the enclosed instructions to become aware of all warnings and maintenance procedures recommended by the manufacturer.


State of the art

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

Specifications

Manufacturer Hu-Friedy
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