Elevator Coupland Number 3C Root Canal File Number 510 Lower Molars - Hu-Friedy - Delynov
The Elévateur Coupland #3C mche #510 molaires du bas - 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 Hu-Friedy Coupland #3C elevator?
The Coupland #3C elevator, manufactured by Hu-Friedy, is a manual surgical instrument specifically designed for the extraction of lower molars. This lower dental elevator is distinguished by its robust configuration adapted to the mechanical stresses of the mandibular area. Developed by Hu-Friedy Mfg. Co., LLC, this tool is part of the surgical consumables category for dentistry. It is intended for the luxation of teeth or roots prior to their final removal. Its design allows for a precise grip for practitioners performing oral surgery procedures. As a Class I medical device, it meets basic regulatory requirements for non-invasive or minimally invasive instrumentation reusable after sterilization.
What are the clinical indications for this instrument?
The lower molar elevator is primarily indicated for the luxation of mandibular molars during simple or complex extraction procedures. Its clinical role is to initiate the expulsion movement of the tooth by creating space between the alveolar wall and the root surface. This molar extraction instrument is particularly useful when the crown is partially decayed or when access for forceps is limited. It allows for tooth mobilization, thus facilitating its removal while preserving the integrity of the surrounding alveolar bone. The use of this Coupland molar elevator is common in daily oral surgery as well as in site preparation for subsequent interventions.
What are the technical characteristics of this elevator?
The Hu-Friedy Coupland #3C elevator features technical characteristics optimized for lower molars. Although composition specifications are not detailed in the source data, this instrument is classified as a Class I medical device. Its morphology, including a #510 handle, is designed to provide an effective lever arm when applying luxation forces. The working part is dimensioned to fit into the periodontal space of lower molars. As a Hu-Friedy product, it benefits from the manufacturing expertise of Hu-Friedy Mfg. Co., LLC, ensuring compliance with professional health standards.
What are the contraindications for the use of this instrument?
According to information from the manufacturer Hu-Friedy Mfg. Co., LLC, specific indications and contraindications must be consulted in the instructions for use attached to the product. From a general clinical perspective, the use of this lower extraction instrument is contraindicated in patients with severe local bone pathologies or mandibular fragilities that increase the risk of fracture when applying leverage force. It is imperative that the practitioner assesses bone density and the proximity of sensitive anatomical structures, such as the inferior alveolar nerve, before any manipulation. Use is strictly reserved for qualified healthcare professionals.
What are the precautions for use and maintenance?
As this instrument is a Class I medical device, it requires a rigorous decontamination and sterilization protocol between each patient, in accordance with Hu-Friedy guidelines. The practitioner must carefully read the manual before use to ensure patient safety and the longevity of the tool. The condition of the working part should be checked before each procedure to detect any wear or deformation. The application of excessive force must be avoided to prevent damage to periodontal tissues or alveolar bone. Storage must be carried out in a dry and clean environment, following the recommendations of the manufacturer located in Chicago, USA.
Who is the manufacturer and what standards are respected?
The Coupland #3C elevator is manufactured by Hu-Friedy Mfg. Co., LLC, with headquarters located at 3232 N. Rockwell St., Chicago, IL 60618, USA. This medical device is classified as Class I according to current regulations. The manufacturer specifies that the use of this instrument is exclusively reserved for healthcare professionals. Although specific CE marking is not mentioned in the source data, the product meets the quality standards associated with the Hu-Friedy brand, recognized in the dental instrumentation sector. Users are encouraged to systematically refer to the official technical documentation provided by the manufacturer for any normative details.
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Specifications
| Manufacturer | Hu-Friedy |
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