Arch Wire Pliers 0.022 inches x 0.025 inches - 1.78 mm - Hu-Friedy - Delynov
The Pince à arcs<=0.022 inch x 0.025 inch arc 1,78mm - 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.
What are the Hu-Friedy archwire forceps?
The Hu-Friedy archwire forceps are a manual instrument specifically designed for practitioners involved in orthodontics and oral surgery. This device allows for the highly rigorous manipulation of archwires whose dimensions do not exceed 0.022 inch x 0.025 inch. Its structure is adapted to meet the requirements of healthcare professionals seeking a reliable tool for managing 1.78mm archwires. Manufactured by Hu-Friedy Mfg. Co., LLC, these forceps are included in the category of GBR (Guided Bone Regeneration) and specialized surgery instruments, offering a response adapted to the needs of bending and shaping orthodontic wires.
What are the clinical indications for this instrument?
This instrument is indicated for all clinical procedures requiring the bending, twisting, or adjustment of orthodontic archwires. As archwire bending forceps, they are used to shape metal wires to the patient's anatomical specificities or to the therapeutic objectives set by the dental surgeon. Their use is strictly reserved for qualified healthcare professionals. They find their primary application in the finishing or alignment phases where the precision of the movement is decisive for the effectiveness of the treatment. The manufacturer Hu-Friedy specifies that the intended use must comply with the clinical protocols in force in dental offices or hospital settings.
What are the technical characteristics of the archwire forceps?
The Hu-Friedy archwire forceps feature technical characteristics calibrated for rectangular or square section archwires. They are specifically dimensioned to accept archwires up to 0.022 inch x 0.025 inch, with a working capacity of 1.78mm. This medical device belongs to Class I according to current regulations. The design of the instrument by Hu-Friedy Mfg. Co., LLC ensures adequate force transmission to bend orthodontic alloys without altering their mechanical properties. Its geometry allows access to different areas of the dental arch to perform intra-oral or extra-oral adjustments according to clinical management needs.
What are the contraindications for the use of this device?
According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not exhaustively listed beyond the requirement for use by a trained healthcare professional. However, the use of these forceps on archwires exceeding the maximum dimensions of 0.022 inch x 0.025 inch is prohibited to avoid any deformation of the instrument or wire breakage. This device should also not be used for functions other than those intended (bending and manipulation of archwires), such as cutting large-diameter wires if the instrument is not equipped with specific cutting inserts, in order to preserve the integrity of the jaws.
What are the maintenance and handling precautions?
As a non-resorbable Class I instrument, the archwire bending forceps require a rigorous sterilization and maintenance protocol after each use. Although composition details are not specified, Hu-Friedy instruments must be cleaned, disinfected, and sterilized in accordance with the instructions in the manual before any new intervention. It is imperative to check the condition of the jaws and the joint before use to guarantee patient safety. Practitioners must carefully read the manual provided by the manufacturer Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA, to ensure the longevity of the instrument and maintain its technical performance during archwire manipulations.
Who is the manufacturer and what standards are respected?
The orthodontic archwire forceps are manufactured by Hu-Friedy Mfg. Co., LLC, a recognized manufacturer in the field of dental instrumentation, based in Chicago, USA. This medical device is classified as Class I, meeting the basic regulatory requirements for reusable surgical instruments. Compliance with the manufacturer's indications and warnings is essential to ensure clinical use conformity. As a product distributed by Delynov, this instrument benefits from the regulatory monitoring associated with devices in its category. Professionals must ensure they consult the labeling and the accompanying manual to confirm the terms of use and the safety standards applied by Hu-Friedy.
State of the art
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Specifications
| Manufacturer | Hu-Friedy |
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