5-angle round scalpel handle (10-130-05A) Compatible with standard blades - Hu-Friedy - Delynov

What is the 10-130-05A round scalpel handle?

The 5-angle round scalpel handle, referenced under code 10-130-05A, is a surgical instrument from the Hu-Friedy brand. This device is specifically designed to accommodate standard scalpel blades used in dental and maxillofacial surgery. Its structure is distinguished by a round-shaped body, offering a different grip than traditional flat handles, and integrates a series of five angles at its shank. This particular design allows the practitioner to adapt the blade orientation according to the needs of the intervention, ensuring precise manipulation of soft tissues during initial incision or dissection phases.

What are the clinical indications for this scalpel blade holder?

This angled scalpel handle is indicated for all oral surgery procedures requiring high cutting precision. It is particularly useful in periodontology for flap procedures, in implantology for crestal or relief incisions, as well as in general oral surgery. Its round shape and five adjustment angles allow reaching posterior sectors or complex anatomical areas where a classic straight handle would limit visibility or the axis of approach. This Hu-Friedy device is exclusively reserved for use by qualified healthcare professionals, in accordance with the manufacturer's directives.

What are the technical characteristics of the Hu-Friedy 10-130-05A handle?

The Hu-Friedy 10-130-05A round scalpel handle features technical specifications oriented towards clinical versatility. Its main feature lies in its 5-angle system, allowing the blade to be positioned at several inclinations to adapt to the morphology of the surgical site. It is compatible with standard scalpel blades on the market. As a Class I instrument, it meets the basic regulatory requirements for non-invasive or temporary-use invasive medical devices. Manufacturing is carried out by Hu-Friedy Mfg. Co., LLC, guaranteeing a recognized production standard in the surgical instrumentation sector.

What are the contraindications for the use of this dental surgery scalpel handle?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not detailed beyond the intended use. However, the use of this handle is strictly reserved for healthcare professionals trained in surgical techniques. An implicit contraindication lies in the use of non-standard blades that would not be compatible with the handle's fixation mechanism, which could compromise the safety of the surgical act. It is imperative to carefully read the instructions for use and respect sterilization protocols before any intervention to prevent infectious risks.

What are the precautions for use and maintenance for this non-resorbable device?

Although the term resorption does not apply to metallic instrumentation, this scalpel handle as a reusable device requires strict precautions. Before each use, the practitioner must check the integrity of the blade fixation mechanism and the absence of corrosion. Cleaning and sterilization must be performed according to Hu-Friedy's rigorous instructions to maintain the mechanical properties of the instrument. Particular attention should be paid to the articulated or angled areas of the 10-130-05A handle to guarantee total decontamination. Compliance with these steps is essential to ensure the longevity of the instrument and patient safety.

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

The official manufacturer of this scalpel handle is Hu-Friedy Mfg. Co., LLC, located in Chicago, USA. This medical device is classified as Class I according to current regulations. Hu-Friedy is a globally recognized manufacturer for the quality of its dental surgery instrumentation. The product must be used in accordance with the warnings and indications provided by the manufacturer. It is specified that healthcare professionals must read the manual carefully before any use. Although specific CE marking is not mentioned in the source data, the Class I status confirms its registration as a regulated medical device.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.