Atraumair #36 extraction forceps, Lower Canines and Incisors, diamond-coated - Hu-Friedy - Delynov

What is the Hu-Friedy Atraumair #36 forceps?

The Atraumair #36 forceps is a precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. It belongs to the category of surgical consumables for dentistry. This specific model is designed for the extraction of anterior teeth of the mandible. Its structure is distinguished by a diamond finish on the beaks, a technical feature aimed at increasing friction and stability when gripping the tooth. As a Class I medical device, it meets the regulatory requirements for non-invasive or invasive instruments for temporary use in dental offices or hospital settings.

What are the clinical indications for these forceps?

This device is specifically indicated for exodontia procedures involving lower canines and incisors. In oral and implant surgery, the practitioner uses the lower canine and incisor forceps to perform the avulsion of the tooth after syndesmotomy. The use of the Atraumair #36 forceps is particularly relevant when the clinician seeks a firm grip on the buccal and lingual surfaces of the anterior mandibular teeth. These lower canine forceps allow for the transmission of the forces necessary for alveololysis while minimizing the risk of slipping on the enamel or dentin, thus facilitating the surgical gesture during simple or complex extractions.

What are the technical characteristics of this instrument?

The Atraumair #36 forceps from the Hu-Friedy brand features an ergonomics adapted to the anatomy of the mandibular anterior teeth. Its main technical characteristic lies in the diamond coating of its beaks. This surface treatment is applied to optimize contact between the instrument and the root or coronal surface, offering superior grip compared to standard forceps. The design of the hinge and handles allows for precise control of the force applied by the dental surgeon. Manufactured by Hu-Friedy Mfg. Co., LLC, this Class I instrument is designed to withstand repeated sterilization cycles in compliance with the manufacturer's maintenance protocols.

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 this instrument is strictly reserved for qualified healthcare professionals. General clinical contraindications apply, notably use on anatomical structures not intended by the instrument's design, such as molars or maxillary teeth, which could lead to a fracture of the tooth or the instrument. Reference should systematically be made to the instructions for use and manufacturer warnings located at 3232 N. Rockwell St. Chicago, Il 60618 USA before any intervention to ensure the suitability between the tool and the patient's clinical situation.

What are the maintenance precautions for these non-resorbable forceps?

As a reusable and non-resorbable metallic surgical instrument, the Atraumair #36 forceps requires a rigorous decontamination and sterilization protocol after each use. The practitioner must follow Hu-Friedy's instructions for manual or ultrasonic cleaning to preserve the integrity of the diamond part. Inadequate cleaning could lead to an accumulation of biological debris reducing grip effectiveness. It is imperative to read the instructions carefully before use to know the recommended sterilization cycles and compatible cleaning products, thus guaranteeing the longevity of the instrument and the aseptic safety of patients in dental surgery.

Who is the manufacturer and what standards are respected?

The Atraumair #36 forceps is manufactured by Hu-Friedy Mfg. Co., LLC, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This manufacturer is globally recognized for the quality of its dental instrumentation. The product is classified as a Class I medical device according to current regulations. Compliance with this regulatory class ensures that the instrument has been designed according to strict safety and performance standards for professional use. Users must comply with the manufacturer's indications and warnings and consult the technical documentation provided to guarantee use in accordance with public health requirements.

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Surgical medical consumables play a decisive role in operative safety.