Elevator #77R M #510 mol. Max/sup Serrated - Hu-Friedy - Delynov

What is the elevator #77R M #510 mol. Max/sup Serrated?

The elevator #77R M #510 mol. Max/sup Serrated is an oral surgery instrument manufactured by Hu-Friedy Mfg. Co., LLC. It belongs to the category of consumables and manual instruments intended for daily clinical practice. This device is distinguished by its specific design for the upper maxillary sector, integrating a serrated handle that ensures a stable grip when applying leverage forces. As a Hu-Friedy product, it benefits from the expertise of a recognized manufacturer in the field of dental instrumentation, guaranteeing a tool adapted to the requirements of dental surgeons for the manipulation of hard tissues and tooth mobilization.

What are the clinical indications for this instrument?

This upper dental elevator is primarily indicated for the luxation of molars in the maxilla. In oral and implant surgery, its role is crucial during the initial phase of extraction, where it serves to separate the tooth from its socket by breaking the periodontal ligament fibers. The use of this instrument allows for the effective mobilization of the molar, thus facilitating the subsequent step of avulsion with forceps. It is particularly suited for procedures requiring precise access to posterior upper areas, where the instrument's configuration allows for the application of necessary pressure with control.

What are the technical specifications of this elevator?

The elevator #77R M #510 is characterized by a working part designed for the anatomy of upper molars. Its serrated handle is a major technical specificity, offering a surface texture that improves the practitioner's tactile control, even in wet conditions. The technical reference #510 corresponds to a precise configuration within the Hu-Friedy range, ensuring a match between the applied force and the resistance of the instrument. This device is classified as a Class I instrument according to current regulatory standards, confirming its status as a medical device intended for professional use in dental offices or hospital environments.

What are the contraindications for the use of this instrument?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. General contraindications include any clinical situation where the application of leverage force could compromise the integrity of adjacent bone structures or neighboring healthy teeth. Reference should systematically be made to the instructions for use and standard clinical recommendations to evaluate if the patient's health status or the anatomical configuration of the area to be treated presents specific risks. The practitioner must ensure that the instrument is used in accordance with its intended use in the upper maxilla.

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

As a non-resorbable metallic surgical instrument, this Hu-Friedy elevator requires a rigorous sterilization and cleaning protocol after each use. Although specific material details are not listed, instruments in this category must be processed according to standard decontamination cycles for Class I devices. It is imperative to read the instructions carefully before use to comply with the cleaning parameters recommended by Hu-Friedy. Regular inspection of the working part and the serrated handle is recommended to detect any signs of wear or metal fatigue, thus ensuring patient safety and the effectiveness of the surgical procedure.

Who is the manufacturer and what standards are met?

The elevator is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed as Class I, meeting the basic regulatory requirements for manual surgical instruments. As a globally recognized manufacturer, Hu-Friedy ensures the traceability and compliance of its products intended for healthcare professionals. Compliance with Class I indicates that the instrument meets the safety and performance criteria defined for this category. Practitioners are invited to consult the manufacturer's warnings and instructions to guarantee use in accordance with modern dental surgery standards.

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Surgical medical consumables play a decisive role in operative safety.