Distributor Number GP2 Sleeve Number 30 0.25/25mm - Hu-Friedy - Delynov

What is the Hu-Friedy Spreader #GP2 handle #30?

The Spreader #GP2 is a high-precision manual endodontic instrument manufactured by Hu-Friedy. This device, identified under technical reference 0,25/25mm, is mounted on an ergonomic type #30 handle. It is specifically designed for root canal obturation procedures. Its structure is optimized for lateral condensation, allowing the practitioner to exert controlled pressure on the filling materials. As a Class I instrument, it meets the rigorous quality requirements imposed by Hu-Friedy Mfg. Co., LLC for non-invasive or short-term invasive medical devices used in dental practices.

What are the clinical indications for this instrument?

The Hu-Friedy Spreader #GP2 is indicated during the final phase of endodontic treatment, specifically during the obturation of root canals. Its primary role is to facilitate the lateral condensation of gutta-percha. By inserting the fine 0,25mm tip into the previously shaped and disinfected canal, the dental surgeon creates lateral space along the master gutta-percha cone. This action allows for the successive insertion of accessory cones, thereby ensuring a hermetic three-dimensional obturation that prevents periapical reinfections. It is used exclusively by qualified healthcare professionals.

What are the technical characteristics of the Spreader #GP2?

This Hu-Friedy instrument features precise technical specifications to meet the constraints of root canal anatomy. The Spreader #GP2 has an active tip with a diameter of 0,25mm and a working length of 25mm. These dimensions are crucial for reaching the apical third of long roots without compromising the integrity of the radicular dentin. The #30 handle provides a stable grip, essential for condensation maneuvers that require both firmness and tactile sensitivity. The design by Hu-Friedy Mfg. Co., LLC guarantees the flexural strength necessary to navigate moderate canal curvatures.

What are the contraindications for the use of this device?

Specific contraindications for the Hu-Friedy Spreader #GP2 are not exhaustively listed in the provided technical documentation, beyond the manufacturer's general warnings. However, the use of this instrument is contraindicated in patients with canal morphologies incompatible with the tip dimensions (0,25/25mm), such as extremely calcified canals or major root resorptions. It must not be used by individuals who have not received adequate training in endodontics. Compliance with sterilization protocols is imperative to avoid any risk of cross-contamination, in accordance with Hu-Friedy instructions.

What are the precautions for use and maintenance?

As with any Class I instrument intended for dental surgery and endodontics, the Hu-Friedy Spreader #GP2 requires careful handling. Before each use, the practitioner must inspect the 0,25mm tip for any signs of metal fatigue, twisting, or corrosion. Excessive pressure during lateral condensation must be avoided to prevent the risk of vertical root fracture. Regarding maintenance, it is imperative to scrupulously follow the instructions from the manufacturer Hu-Friedy Mfg. Co., LLC for cleaning, disinfection, and autoclave sterilization, in order to preserve the mechanical properties of the steel and the longevity of the instrument.

Who is the manufacturer and what standards are respected?

The Spreader #GP2 handle #30 is manufactured by Hu-Friedy Mfg. Co., LLC, located in Chicago, 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. Although specific CE marking is not mentioned in the source data, compliance with Hu-Friedy manufacturing standards ensures conformity with safety and performance requirements for medical devices. Healthcare professionals must imperatively read the instructions for use provided by the manufacturer before any clinical intervention to ensure compliant usage.

State of the art

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