Elevator Coupland Number 2C with Handle Number 510 - Hu-Friedy - Delynov

What is the Coupland #2C elevator with #510 handle?

The Coupland #2C elevator with #510 handle is a high-quality surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This extraction equipment device is specifically designed for oral surgery procedures requiring effective luxation of dental structures. It consists of a Coupland #2C active part and an ergonomic handle referenced as #510, optimizing grip during force maneuvers. As a Class I medical device, it meets regulatory requirements for use in professional clinical environments. The robust design ensures adequate force transmission to facilitate extraction while respecting the integrity of surrounding tissues.

What are the clinical indications for this Hu-Friedy instrument?

The Coupland #2C elevator is indicated for the luxation of teeth, roots, and root fragments during simple or complex extractions. Its use is particularly relevant in oral surgery and implantology to prepare the alveolar site before avulsion. The instrument allows for widening the socket and breaking ligament attachments through leverage or rotational movements. This extraction equipment is reserved exclusively for healthcare professionals trained in dental surgical techniques. The manufacturer Hu-Friedy specifies that the intended use must strictly follow current clinical protocols to guarantee patient safety and the effectiveness of the operative procedure.

What are the technical characteristics of this elevator?

This instrument is distinguished by the combination of the Coupland #2C tip and the #510 handle. Manufactured by Hu-Friedy, a recognized manufacturer in the field of surgical instrumentation, this elevator is classified as a Class I device. Although specific materials are not detailed in the technical sheet, manufacturing by Hu-Friedy Mfg. Co., LLC guarantees a high quality standard for repeated interventions. The #510 handle is designed to offer maximum stability to the practitioner, allowing for precise application of the leverage forces necessary when using this extraction equipment in a surgical setting.

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 elevator is strictly reserved for qualified healthcare professionals. General contraindications include the use of the instrument for procedures not intended by the manufacturer or by untrained individuals. Although the raw MDR text does not list specific medical contraindications related to allergies or systemic pathologies, the practitioner must evaluate the patient's clinical status before any intervention. It is imperative to read the instructions carefully before use to ensure the device is suitable for the clinical case being treated and to avoid any technical misuse.

What are the maintenance precautions for this non-resorbable equipment?

As this is a reusable metallic surgical instrument and not a suture, precautions mainly concern the sterilization and maintenance cycle. This extraction equipment must be cleaned, disinfected, and sterilized before each use in accordance with Hu-Friedy manufacturer instructions. As a Class I device, it must undergo regular inspection to detect any signs of wear or metal fatigue that could compromise its integrity during luxation. Compliance with decontamination protocols is essential to prevent cross-infections in the dental office and ensure the longevity of the surgical instrumentation.

Who is the manufacturer and what standards are respected?

The Coupland #2C elevator with #510 handle is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 in the USA. This device is classified as Class I according to medical device regulations. Hu-Friedy is a manufacturer recognized for its expertise in producing precision surgical instruments. The product is intended exclusively for professional use by healthcare practitioners. It is reminded that it is necessary to consult the technical instructions and follow the manufacturer's warnings to ensure use compliant with the safety and clinical efficacy standards required for this type of extraction equipment.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.