Ligature director number 2 with handle number 41 of 1.10mm retro - Hu-Friedy - Delynov

What is the plugger #2 handle #41 1.10mm retro - Hu-Friedy?

The plugger #2 handle #41 1.10mm retro is a specialized manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. It consists of a 1.10mm working part mounted on a number 41 handle. This device is specifically developed for endodontic surgery procedures, more precisely for the filling phases after an apical resection. As a precision instrument, it allows the practitioner to compact filling materials in restricted access areas. Hu-Friedy's manufacturing quality ensures an instrument adapted to the requirements of daily clinical practice in oral surgery or exclusive endodontics offices.

What are the clinical indications for this retro plugger?

The use of this endodontic retro plugger is indicated during endodontic surgeries requiring a retro filling. After performing an apicoectomy and preparing a Class I cavity at the root apex, this retro plugger allows for the rigorous condensation of filling materials, such as MTA or other bioceramic cements. Its 1.10mm diameter is adapted to the dimensions of standard apical preparations, ensuring optimal sealing of the retrograde filling to prevent peri-apical infectious recurrences.

What are the technical characteristics of this instrument?

The plugger #2 handle #41 is distinguished by an active tip calibrated at 1.10mm, a critical dimension for insertion into micro-cavities prepared by ultrasound during retro endo surgery. The #41 handle offers a stable grip for precise tactile control during the pressure exerted on the filling material. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets the brand's quality standards. It belongs to the category of manual diagnostic and treatment instruments in surgical endodontics, offering resistance adapted to the condensation forces necessary for a retro filling instrument.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy, the use of this instrument is reserved exclusively for qualified healthcare professionals. There are no specific medical contraindications listed in the raw documentation, other than general contraindications related to endodontic surgery procedures. The practitioner must assess the patient's general health status and ensure the absence of allergies to the metallic components of conventional surgical instrumentation before any intervention. It is imperative to read the instructions for use carefully before any clinical manipulation.

What are the maintenance precautions for this endo retro plugger?

This endo retro plugger is a non-absorbable and reusable instrument that requires a strict sterilization protocol between each patient. Although material specifications are not detailed in the source text, Hu-Friedy Class I instruments must be cleaned, disinfected, and sterilized according to current hospital or office protocols (autoclave). The integrity of the 1.10mm tip should be checked before each use to guarantee condensation efficiency. Careful handling prevents deformation of the working part, which is essential for the precision of the retro filling.

Who is the manufacturer and what standards are respected?

The product is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. As a recognized manufacturer, Hu-Friedy ensures the compliance of its instruments with the safety and performance requirements for medical devices of this class. Practitioners must refer to the manufacturer's instructions to ensure use in accordance with health safety standards. Compliance with Class I highlights that this instrument meets the basic criteria for non-invasive or invasive devices for temporary use.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.