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Mirror Handle Number 7 American Thread - Hu-Friedy - Delynov

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The Manche de Miroir manche #7 pas-de-vis améric. - 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.

33.75 € 33.75 EUR 33.75 € Tax Included

33.75 € Tax Included

(0.00 € / Units)
  • Manufacturer

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Instrument

What is the Hu-Friedy #7 mirror handle?

The #7 mirror handle produced by Hu-Friedy is a support instrument designed to receive interchangeable mirror heads. This device is distinguished by its specific architecture and standardized fixation system. Manufactured by Hu-Friedy Mfg. Co., LLC, this accessory is a central element of rotary and manual office instrumentation. Its design is optimized to offer a grip adapted to the requirements of oral surgery, allowing the practitioner to manipulate the assembly with the necessary stability during clinical exploration phases. This model respects the manufacturing standards of the brand, recognized for the quality of its devices in the dental and surgical sector.

What are the clinical indications?

The surgical mirror handle is indicated for all oral surgery, implantology, and periodontology procedures requiring indirect vision or retraction of soft tissues (cheeks, tongue, flaps). Its use is systematic during initial examinations, preparation of implant sites, or verification of osteotomy. As a support, it allows for precise positioning of the mirror to illuminate shadow areas or visualize distal and palatal/lingual surfaces. This device is essential for maintaining optimal visibility throughout the operative act, thus guaranteeing the safety and precision of the surgical gesture in restricted access areas of the oral cavity.

What are the technical characteristics?

This mirror handle features specific technical characteristics, notably an American thread. This threading specificity is crucial when purchasing a mirror handle because it determines compatibility with mirror heads available on the market. The #7 format corresponds to a precise handle morphology, studied for balance and control during use. This product belongs to the GBR (Guided Bone Regeneration) category within the Delynov catalog, although it is a transversal instrument across all disciplines. Manufacturing is ensured by Hu-Friedy Mfg. Co., LLC, guaranteeing compliance with health professional requirements for manual diagnostic instruments.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-Friedy, there are no documented specific medical contraindications for the use of this handle other than those related to the general use of metallic instrumentation in the oral environment. However, the use of this American thread mirror handle is strictly reserved for qualified healthcare professionals. It is imperative to check the integrity of the thread before each intervention to avoid any risk of the mirror head becoming detached in the mouth. The practitioner must refer to the instructions for use for any additional information relating to the safety and limitations of use of the device.

What are the maintenance and durability precautions?

As a non-resorbable Class I device, the durability of the handle directly depends on compliance with cleaning, disinfection, and sterilization protocols. Although composition details are not specified in the source data, this type of Hu-Friedy instrument is designed to undergo repeated sterilization cycles in an autoclave. It is recommended to carefully clean the thread to remove any biological residue or tartar debris that could compromise the fixation of the mirror head. Regular inspection of the surface condition and the threading is necessary to guarantee the longevity of the instrument and patient safety during clinical examinations.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device. In accordance with current regulations, this equipment is exclusively reserved for professional use. The manufacturer insists on the need to read the instructions carefully before any use. Although specific CE marking is not mentioned in the source data, belonging to Class I indicates that the product meets safety and performance requirements for basic surgical instruments. The reliability of Hu-Friedy ensures traceability and compliance with American and international industrial standards.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

Specifications

Manufacturer Hu-Friedy
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