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Allen Periosteal Elevator, anterior, Black Line - Hu-Friedy - Delynov

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The Décolleur Élévateur Allen, antérieur, Black Line - 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.

154.20 € 154.2 EUR 154.20 € Tax Included

154.20 € Tax Included

(0.00 € / Units)
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Instrument

What is the Black Line Allen anterior periosteal elevator?

The Allen periosteal elevator, anterior version, belongs to the Black Line range developed by Hu-Friedy. It is a specialized hand instrument for oral surgery, designed to manipulate soft tissues with great finesse. Its structure is optimized for the anterior areas of the oral cavity. As an instrument in the INSTRU category, it meets the manufacturing requirements of Hu-Friedy Mfg. Co., LLC, a recognized manufacturer in the field of periodontal and implant instrumentation. This device is specifically developed for practitioners requiring a reliable tool for the preparation of full-thickness or partial-thickness flaps.

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

This instrument is primarily indicated for periodontal plastic surgery and implant surgery procedures in the anterior sector. It is used by dental surgeons for periosteal elevation and the detachment of gingival tissues to clear the alveolar bone. Its use is particularly relevant during the creation of tunnels, the placement of connective tissue grafts, or during site preparation before implant placement. The intended use, as defined by the manufacturer Hu-Friedy, is strictly reserved for qualified healthcare professionals mastering advanced oral surgery techniques.

What are the technical characteristics of this elevator?

The Allen anterior periosteal elevator is distinguished by its membership in the Hu-Friedy Black Line series, characterized by a specific coating that improves visual contrast at the surgical site and reduces reflections under the surgical light. Although the exact composition is not specified in the technical data, the design is focused on clinical performance in a surgical environment. This instrument is classified as a Class I medical device, guaranteeing its compliance with safety standards for non-invasive or short-term reusable instruments. Its shape is designed to offer precise handling during the dissection of delicate tissues.

What are the contraindications for the use of this device?

According to the information provided by Hu-Friedy Mfg. Co., LLC, specific contraindications are not exhaustively listed beyond standard warnings related to professional use. However, the use of this instrument is contraindicated for any person who is not a qualified healthcare professional. It is also necessary to respect sterilization and maintenance protocols to avoid any risk of cross-contamination or mechanical failure. The practitioner must refer to the instructions for use to verify the suitability of the instrument with the patient's physiological state and the specific nature of the planned surgical intervention.

What are the precautions for use and maintenance?

As a Class I non-resorbable instrument, precautions for use are based on careful handling to preserve the integrity of the active ends. Hu-Friedy recommends a careful reading of the instructions before any use. The instrument must be cleaned, disinfected, and sterilized according to the protocols in force in dental practices before each use. It is essential to check for the absence of visible damage before the intervention. As this is a device reserved for healthcare professionals, its handling must respect the rules of the art of periodontal surgery to avoid any unintentional tissue injury during flap detachment.

Who is the manufacturer and what standards are respected?

The Allen periosteal elevator 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 instrumentation. This product is a Class I medical device. Compliance with Hu-Friedy's manufacturing protocols ensures that the instrument meets the regulatory requirements for use in oral surgery. Although specific CE marking is not mentioned in the source data, the Class I classification indicates compliance with safety and performance rules applicable to reusable manual surgical instruments.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Hu-Friedy
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