Elevator Cryer no.45 Gr no.510 right small - Hu-Friedy - Delynov

What is the Cryer #45 Gr #510 right small elevator?

The Cryer #45 Gr #510 right small elevator is a manual surgical instrument developed by the manufacturer Hu-Friedy. This device is specifically designed for oral surgery procedures requiring the extraction of roots or dental debris. It belongs to the category of consumables and precision instruments for exodontia. As a small cryer elevator, its structure is adapted to restricted spaces, offering optimized handling for practitioners. This model is intended for strict professional use in a clinical or hospital environment. Its design meets the quality requirements of the Hu-Friedy brand, recognized for its high-precision instruments.

What are the clinical indications?

The use of this instrument is indicated for dental extraction procedures, specifically for the removal of persistent roots and bone or dental fragments. The Cryer #45 elevator is particularly useful when the tooth is fractured at or below the gum line. It allows the dental surgeon to apply a controlled leverage force to luxate the root from its alveolar housing. This specific model is oriented for right-side application. It is commonly used during complex oral surgeries or simple extractions requiring mechanical assistance to release dental structures without damaging the surrounding alveolar bone.

What are the technical characteristics?

The Cryer #45 Gr #510 right small elevator is distinguished by its geometric configuration oriented for right-side use. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument is classified as a Class I medical device according to current regulations. Its "small" size allows for precise insertion into the socket, minimizing bulk during surgical maneuvers. Although specific material details are not provided in the source data, the instrument adheres to the rigorous manufacturing standards of Hu-Friedy. It is designed to withstand the mechanical stresses exerted during dental luxation while providing the tactile feedback necessary for the practitioner to assess tissue resistance.

What are the contraindications for use?

In accordance with information from the manufacturer Hu-Friedy, this instrument is exclusively reserved for qualified healthcare professionals. General contraindications include any clinical situation where the application of leverage force could compromise critical anatomical structures, such as the maxillary sinus or the inferior alveolar nerve, without adequate prior planning. Use by untrained personnel is strictly prohibited. It is imperative to refer to the instructions for use and to respect sterilization and asepsis protocols before any intervention. Any systemic pathology of the patient that could interfere with post-extraction healing must be evaluated before using this surgical instrument.

What are the precautions for use?

As a non-resorbable and reusable instrument, this elevator requires rigorous maintenance protocols. Before each use, the practitioner must carefully read the instructions provided by Hu-Friedy. The instrument must be inspected to verify the absence of structural damage or premature wear that could affect its performance or patient safety. As it is a Class I device, it must be cleaned, disinfected, and sterilized according to the recommendations of the manufacturer Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA. Particular attention must be paid to the sharpening of the working part to ensure constant efficiency during the luxation of dental roots.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is a Class I medical device, which implies that it meets the basic regulatory requirements for manual surgical instruments. The Hu-Friedy brand is a recognized manufacturer in the dental sector for its compliance with international manufacturing standards. Although specific CE marking is not mentioned in the source documentation, the device follows strict directives relating to instruments intended for healthcare professionals. Users must ensure the compliance of the instrument with their facility's protocols before any clinical implementation.

State of the art

Surgical medical consumables play a decisive role in operative safety.