Elevator Davis Number 11 with Handle Number 503 - Hu-Friedy - Delynov

What is the Davis elevator #11 handle #2 - Hu-Friedy?

The Davis elevator #11 with handle #2 is a precision manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is specifically designed for oral surgery and implantology procedures. It consists of a Davis #11 type working part mounted on a size #2 ergonomic handle, optimizing grip during luxation maneuvers. As an instrument from the Hu-Friedy brand, it benefits from the expertise of a recognized manufacturer in the field of dental instrumentation. This device is classified as a Class I instrument according to current regulations, guaranteeing its compliance for professional use in dental practices or hospital environments.

What are the clinical indications for this davis elevator?

The dental davis elevator is primarily indicated for simple or complex extraction procedures. In oral surgery and implantology, it is used for the initial luxation of the tooth or root fragments. Its role is to separate the dental element from its alveolar attachment by applying controlled pressure on the periodontal ligament. This instrument is also useful during the preparatory phases of guided bone regeneration (GBR) when an atraumatic extraction is necessary to preserve the bone plates. The use of the Davis elevator #11 allows roots to be mobilized before using a forceps, thereby reducing the risk of root fracture or damage to surrounding tissues.

What are the technical characteristics of this instrument?

The Davis elevator #11 is distinguished by its technical configuration combining a specific tip and a #2 type handle. Manufactured by Hu-Friedy, this instrument meets the requirements of Class I for medical devices. The #11 tip is designed to insert effectively into the periodontal space, while the #2 handle offers a diameter and weight studied to ensure optimal tactile control when applying leverage forces. Although the exact materials are not specified in the source data, manufacturing by Hu-Friedy Mfg. Co., LLC ensures a finishing quality consistent with the high standards of professional dental surgery. The instrument is delivered non-sterile and must be processed according to current sterilization protocols.

What are the contraindications for the use of this instrument?

According to the information provided by the manufacturer Hu-Friedy, the use of this elevator is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed in the raw technical documentation, other than the standard precautions for use related to any surgical instrumentation. However, the use of this davis elevator is contraindicated for any person who does not possess the clinical training required for oral surgery procedures. It is imperative to carefully read the instructions for use and respect the warnings from the manufacturer Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA before any intervention on a patient to prevent any iatrogenic risk.

What are the maintenance and safety precautions?

As a Class I device, the Hu-Friedy Davis elevator #11 requires rigorous maintenance to ensure its longevity and the safety of care. Although this instrument is non-resorbable, it must undergo a full cycle of decontamination, cleaning, and sterilization after each use, in accordance with the directives of the manufacturer Hu-Friedy Mfg. Co., LLC. Professionals must inspect the instrument before each use to detect any signs of wear or deformation of the working tip. Particular attention must be paid to compliance with asepsis protocols to avoid cross-contamination. The manufacturer emphasizes the importance of following the instructions on the leaflet attached to the product to maintain the performance of the davis elevator.

Who is the manufacturer and what standards are met?

The Davis elevator #11 is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This manufacturer is globally recognized for the quality of its surgical instruments. This specific product is listed under Class I of medical devices. Compliance with manufacturing standards by Hu-Friedy ensures that the instrument meets the safety and performance requirements for dental surgery and GBR procedures. Although CE marking is not explicitly specified in the source data, traceability and regulatory compliance are ensured by the clear identification of the manufacturer and its official address in the United States. This device is exclusively reserved for use by trained healthcare professionals.

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