Apical Elevator Heidbrink number 13/14 with Handle number 522 - Hu-Friedy - Delynov

What is the Heidbrink #13/14 apical elevator with #522 handle?

The Heidbrink #13/14 apical elevator is a specialized apical surgery instrument designed by the manufacturer Hu-Friedy. This device consists of a double active part mounted on an ergonomic #522 handle. It is specifically developed for intervention in restricted alveolar areas. As a precision instrument, it allows the practitioner to mobilize root structures with great finesse. The design by Hu-Friedy Mfg. Co., LLC guarantees a tool adapted to the requirements of oral surgery operating blocks. Its robust structure is designed to withstand the mechanical stresses associated with fragment luxation without compromising the integrity of the surrounding alveolar bone.

What are the clinical indications for this instrument?

This instrument is primarily indicated for the extraction of root fragments or fractured apices during complex dental surgeries. It is useful in apical surgery procedures where visual and instrumental access is limited. The use of this Heidbrink #13/14 elevator is recommended for dislodging root debris from the periodontal ligament. It is used by dental surgeons and implantologists in contexts of difficult extractions or alveolar revisions. The manufacturer Hu-Friedy specifies that this device is strictly reserved for healthcare professionals trained in oral and maxillofacial surgery techniques.

What are the technical characteristics of this elevator?

The Heidbrink #13/14 elevator is distinguished by its double active ends, allowing for versatility of approach depending on the angulation required during the intervention. The #522 handle offers a stable grip, essential for applying controlled force during luxation. Manufactured by Hu-Friedy, this instrument meets the brand's quality standards for manual instrumentation. Although the exact composition is not specified in the source data, manufacturing by Hu-Friedy Mfg. Co., LLC ensures compatibility with standard sterilization protocols in a clinical environment. This device is classified as a Class I instrument according to current regulations.

What are the contraindications for the use of this device?

According to information provided by the manufacturer Hu-Friedy, specific contraindications are not detailed beyond the intended use. However, the use of this instrument is formally reserved for qualified healthcare professionals. Inappropriate use by untrained personnel constitutes a major contraindication. As with any apical surgery instrument, its use should be avoided if clinical conditions do not allow sufficient visual control or if the integrity of adjacent anatomical structures, such as the maxillary sinus or the inferior alveolar nerve, risks being compromised by the pressure exerted.

What are the maintenance and handling precautions?

Being a non-resorbable instrument intended for repeated use after reprocessing, this elevator must be cleaned and sterilized before each use. It is imperative to carefully read the instructions provided by Hu-Friedy before any handling. The practitioner must inspect the instrument for any signs of wear or deformation of the Heidbrink #13/14 active tips before the surgical act. Careful handling is required to preserve the precision of the ends. Compliance with decontamination and thermal or chemical sterilization protocols, in accordance with the instructions from the manufacturer Hu-Friedy Mfg. Co., LLC, is essential to guarantee patient safety and the longevity of the tool.

Who is the manufacturer and what standards are respected?

The Heidbrink #13/14 apical elevator 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. The Hu-Friedy brand is recognized in the dental sector for the quality of its surgical instruments. The product is distributed by Delynov and must be used in accordance with the Medical Device Regulation (MDR) directives. Although specific CE marking is not mentioned in the source documentation, compliance with Class I indicates that the instrument meets the essential safety and performance requirements for non-invasive or invasive medical devices for temporary use.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.