Elevator Cryer no. 25 handle no. 510 left medium - Hu-Friedy - Delynov

What is the Cryer #25 elevator #510 handle left medium?

The Cryer #25 elevator is a precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. It consists of a specific working part and a #510 type handle. This instrument, often associated with the family of syndesmotomes or triangular-tipped elevators, is designed to facilitate the extraction of dental roots. Its configuration is optimized for a left lateral approach. As a Class I medical device, it meets the basic regulatory requirements for non-invasive or short-term invasive manual instrumentation. Its robust structure allows for controlled force transmission during luxation, ensuring reliable handling for the practitioner in oral surgery or implantology clinics.

What are the clinical indications for this Hu-Friedy instrument?

This medium cryer elevator is primarily indicated for the extraction of roots, root fragments, or multi-rooted teeth with decayed crowns. In clinical practice, it is used after the use of initial syndesmotomes to luxate the root by taking support on the inter-radicular septum or the alveolar ridge. Its specific design for the left side allows the surgeon to access the corresponding mandibular or maxillary areas with an appropriate angle of attack. It is particularly useful in cases of complex extractions where simple vertical elevation is not sufficient to mobilize the fragment. The use of this instrument is strictly reserved for qualified healthcare professionals mastering exodontia techniques.

What are the technical characteristics of the Cryer #25 elevator?

The Cryer #25 elevator is distinguished by its sharp triangular tip, characteristic of the Hu-Friedy Cryer range. The #510 handle provides a grip adapted to procedures requiring constant leverage. The 'left' designation indicates the orientation of the active face of the tip relative to the handle, allowing for optimal application of force in the desired direction of luxation. Although the exact composition is not specified in the source data, the manufacturing standards of Hu-Friedy Mfg. Co., LLC ensure a high-quality finish specific to Class I medical devices. This instrument is designed to withstand the cleaning and sterilization cycles required in a clinical setting, in accordance with the instructions from the manufacturer located in Chicago.

What are the contraindications for the use of this elevator?

According to the information provided by the manufacturer Hu-Friedy, specific contraindications are not detailed beyond the general scope of the intended use. However, the use of this instrument is formally reserved for healthcare professionals. An obvious clinical contraindication would reside in the use of the instrument on an anatomical area not compatible with the 'left' orientation of the tip, which could lead to damage to soft tissues or adjacent alveolar walls. Furthermore, it must not be used if the integrity of the instrument is compromised or if the practitioner does not have the necessary training to handle triangular-tipped elevators. It is imperative to read the instructions carefully before any use to ensure patient safety.

What are the precautions for use and maintenance?

As a non-resorbable and reusable Class I instrument, the Cryer #25 elevator requires a strict decontamination and sterilization protocol between each patient. The manufacturer Hu-Friedy emphasizes the importance of following warnings and intended use. Precautions include a visual inspection before each intervention to check for the absence of corrosion or deformation of the active tip. Inappropriate use, such as applying excessive torsional force on a bone support that is too thin, can lead to alveolar fractures or damage the instrument. Compliance with the cleaning procedures recommended by Hu-friedy 3232 N. Rockwell St. Chicago is essential to maintain the cutting and leverage performance of the elevator over the long term.

Who is the manufacturer and what standards are respected?

The Cryer #25 elevator is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, IL 60618 USA. This medical device is classified as Class I according to current regulations. Although specific CE marking is not mentioned in the provided technical sheet, the product complies with the rigorous manufacturing standards imposed on medical devices reserved for healthcare professionals. Hu-Friedy is a globally recognized manufacturer for the quality of its surgical instrumentation. Users are invited to consult the instructions for use and to respect the indications and contraindications provided by the manufacturer to ensure practice in accordance with safety and clinical efficacy requirements.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.