Needle holder mayo-hegar num 5042 tungsten carbide 16cm - hu-friedy - delynov

What is the Hu-Friedy Mayo-Hegar #5042 needle holder?

The Mayo-Hegar #5042 needle holder developed by Hu-Friedy is a precision instrument intended for surgery. This model is distinguished by the integration of jaws with tungsten carbide inserts, a material recognized for its hardness and wear resistance. With a length of 16cm, this instrument offers optimal balance for practitioners performing sutures in the oral environment. Manufactured by Hu-Friedy Mfg. Co., LLC, this Class I medical device meets the quality requirements of demanding clinical environments, guaranteeing stable handling of suture needles without risk of slipping during trans-mucosal passage.

What are the clinical indications for this instrument?

This Mayo-Hegar needle holder is indicated for all oral surgery procedures requiring tissue synthesis by suture. It is particularly used in implantology for the closure of surgical sites, in periodontology for flap stabilization, or during complex extractions requiring approximation stitches. Its 16cm length allows access to both posterior and anterior sectors. The use of this instrument is strictly reserved for qualified healthcare professionals, in accordance with the Hu-Friedy manufacturer's guidelines, thus guaranteeing an application compliant with current surgical care standards.

What are the technical characteristics of the Mayo-Hegar #5042 needle holder?

Technically, the Mayo-Hegar #5042 needle holder has a total length of 16cm. Its major feature lies in its reinforced tungsten carbide jaws. These inserts provide an extremely durable textured gripping surface that limits needle rotation, even under stress. The structure of the instrument allows for precise transmission of the force exerted by the surgeon, facilitating the passage of the needle through tissues of varying densities. As a Hu-Friedy product, it benefits from a rigorous design specific to Class I instruments, ensuring constant reliability during repeated use in dental offices or operating rooms.

What are the contraindications for the use of this device?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this needle holder is specifically reserved for healthcare professionals. There are no specific medical contraindications listed in the raw technical documentation, other than the imperative compliance with sterilization and asepsis protocols specific to surgical instrumentation. Reference should systematically be made to the instructions for use before any intervention. The instrument must be used exclusively for its intended purpose, namely the manipulation of suture needles, and must not be diverted for other mechanical functions that could damage the tungsten carbide inserts.

What are the maintenance precautions for this non-absorbable needle holder?

Although the term absorption applies to sutures, the durability of this steel Hu-Friedy needle holder with carbide inserts depends directly on its maintenance. As a non-absorbable and reusable Class I instrument, it must undergo a complete cycle of cleaning, disinfection, and sterilization between each patient. The tungsten carbide inserts, although very resistant, require regular inspection to check for the absence of debris or wear of the gripping pattern. Compliance with the sterilization parameters recommended by Hu-Friedy is essential to maintain the structural integrity of the 16cm instrument and guarantee the safety of care during surgical interventions.

Who is the manufacturer and what standards are met by this product?

The Mayo-Hegar #5042 needle holder is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This device is regulatory classified as Class I according to current standards for reusable surgical instruments. Hu-Friedy is a manufacturer recognized worldwide for the quality of its manual instrumentation. The product is designed to meet the requirements of healthcare professionals, with traceability and compliance with American industrial manufacturing standards. The Class I designation confirms its status as a medical device, implying rigorous technical documentation and compliance with safety and performance requirements for the intended clinical use.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.