Atraumair 67 Extraction Forceps, Upper Molars, diamond-coated - Hu-Friedy - Delynov
The Davier Atraumair 67, Molaires Haut, diamanté - 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 is the Atraumair 67 Hu-Friedy Forceps?
The Atraumair 67 Forceps is an oral surgery instrument developed by Hu-Friedy for dental avulsion. This model is distinguished by its specific configuration adapted to the anatomy of upper molars. It integrates a diamond finish on the beaks, a technical feature aimed at optimizing contact with the tooth surface. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument belongs to the category of reusable surgical consumables. Its robust structure meets the requirements of complex exodontia procedures where instrument stability is paramount for the practitioner.
What are the clinical indications for these upper diamond forceps?
These upper diamond forceps are exclusively indicated for the extraction of molars located in the upper maxilla. In oral surgery, its use is recommended during simple or complex avulsion protocols requiring a firm grip on the crown or the neck of the molar. The main indication concerns dental surgeons and stomatologists performing upper molar extractions in a standard clinical or implant setting. The instrument is designed to adapt to the multi-rooted morphology of upper posterior teeth, thus allowing the application of the luxation forces necessary to rupture the periodontal ligament.
What are the technical characteristics of this instrument?
The Atraumair 67 Forceps from the Hu-Friedy brand features specific technical characteristics for surgery. Its working part is equipped with a diamond coating, a specificity that increases friction between the steel and the tooth, thereby reducing the risk of slippage during rotation or tilting movements. These upper molar forceps are classified as a Class I medical device, in accordance with current regulations. The Atraumair design aims to offer precise handling while respecting the integrity of the surrounding tissues when accessing the posterior sectors of the maxilla.
What are the contraindications for the use of this device?
According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of these forceps is strictly reserved for qualified healthcare professionals. Clinical contraindications are not specifically detailed in the raw documentation, but the use of the device must comply with the general indications and contraindications of exodontia. It is imperative to consult the instructions for use provided by the manufacturer Hu-Friedy before any intervention. As with any surgical instrument, a preoperative evaluation of the condition of the tooth and supporting tissues is necessary to validate the relevance of using these specific forceps.
What are the maintenance and handling precautions?
As the Atraumair 67 forceps is a non-resorbable instrument intended for surgery, it requires a rigorous sterilization protocol between each patient. Although material specifications are not detailed, this type of oral surgery instrument must be handled with care to preserve the diamond coating of the beaks. Professionals must ensure that the instrument is free of debris before sterilization. It is reminded that this device is reserved for professional use and that compliance with the warnings from the manufacturer Hu-Friedy, located in Chicago, is essential to guarantee the safety of care and the longevity of the tool.
Who is the manufacturer and what standards are respected?
The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, whose headquarters is located at 3232 N. Rockwell St. Chicago, IL 60618 USA. These forceps are listed as a Class I medical device. Compliance with manufacturing standards by Hu-Friedy ensures that the instrument meets the safety and performance requirements for dental surgery procedures. As a Class I product, it follows the declaration of conformity procedures applicable to reusable surgical instruments. Practitioners must systematically refer to the labeling and instructions to confirm the methods of use in accordance with the manufacturer's directives.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Hu-Friedy |
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