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Apical Elevator Howard #2/3 with Handle #522 - Hu-Friedy - Delynov

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The Elévateur Apical Howard #2/3 manche #522 - Hu-Friedy is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.

  • Compliance: Medical device Class I.
  • Manufacturer: Hu-Friedy Mfg. Co., LLC.
  • Reserved for healthcare professionals. Read instructions carefully before use.

113.85 € 113.85 EUR 113.85 € Tax Included

113.85 € Tax Included

(0.00 € / Units)
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Instrument

What is the Howard #2/3 apical elevator with #522 handle?

The Howard #2/3 apical elevator, combined with the #522 handle, is a high-quality manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is specifically designed for oral surgery procedures requiring the elevation or luxation of dental structures, particularly at the apical level. As an instrument in the INSTRU category, it benefits from the expertise of Hu-Friedy, a recognized manufacturer in the field of dental instrumentation. Its structure is adapted to the requirements of clinicians seeking a reliable tool for delicate interventions. This product is classified as a Class I medical device, meeting the basic regulatory requirements for non-invasive or reusable instruments after sterilization.

What are the clinical indications?

This Howard #2/3 elevator is indicated for exodontia and oral surgery procedures. Its primary use concerns the elevation of root fragments and apices, thereby facilitating their removal during difficult extractions or alveolar revision surgeries. It is particularly useful in situations where access is restricted and where controlled force is necessary to break ligamentous attachments. The instrument is exclusively reserved for qualified healthcare professionals, such as dental surgeons and implantologists, who master apical elevation techniques to minimize trauma to surrounding tissues.

What are the technical characteristics?

The Howard #2/3 elevator is distinguished by its specific Howard configuration, optimized for work in apical areas. It is mounted on a handle with reference #522, designed by Hu-Friedy to provide a grip adapted to the requirements of oral surgery. Although precise materials are not specified in the provided technical documentation, the manufacturing standards of Hu-Friedy Mfg. Co., LLC guarantee an instrument meeting the sterilization and durability needs required in a dental office. As a Class I device, it follows a rigorous manufacturing protocol in compliance with safety standards for manual surgical instruments.

What are the contraindications for use?

According to information from the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for healthcare professionals. Clinical contraindications are not explicitly listed in the source documentation, but the use of this elevator must be avoided by any person not trained in dental surgical techniques. Standard oral surgery protocols must be respected, and it must be ensured that the patient's health status allows for the planned intervention. The practitioner must systematically read the instructions and warnings carefully before any use to ensure patient safety and the integrity of the device.

What are the maintenance and safety precautions?

Like any Class I instrument intended for surgery, the Howard #2/3 elevator must be handled with care. It is imperative to follow the cleaning and sterilization instructions provided by Hu-Friedy to maintain the instrument in optimal working condition and prevent risks of cross-contamination. Before each intervention, the practitioner must inspect the instrument to check for the absence of visible damage. Use must comply with the intended use by the manufacturer located at 3232 N. Rockwell St. Chicago, USA. Particular attention must be paid when handling active parts to avoid any accidental injury or deterioration of the apical tip.

Who is the manufacturer and what standards are met?

The Howard #2/3 apical elevator is manufactured by Hu-Friedy Mfg. Co., LLC, whose headquarters are located in Chicago, Illinois, USA. This medical device belongs to Class I. Compliance with manufacturing standards by Hu-Friedy ensures that the instrument conforms to the regulatory requirements applicable to medical devices in this category. Although specific CE marking is not mentioned in the source data, the product follows the safety and performance directives defined for surgical instruments reserved for healthcare professionals. Clinicians can refer to the manufacturer's contact details for any additional information on compliance.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
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