Jovanovic Plugger, Black Line - Hu-Friedy - Delynov

What is the Jovanovic plugger, Black Line - Hu-Friedy?

The Jovanovic plugger, from the Black Line collection by the brand Hu-Friedy, is a high-precision surgical instrument intended for the manipulation of filling materials. This device is distinguished by its specific Black Line coating, designed to improve visual performance and reduce reflections during interventions under intense operating lighting. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument is specifically structured to meet the requirements of dental surgeons and implantologists practicing guided bone regeneration. Its robust design and meticulous finish make it a tool of choice for the transfer and compaction of biomaterials in alveolar areas.

What are the clinical indications for the Jovanovic plugger?

The jovanovic plugger is mainly indicated for bone grafting procedures and bone surgery in the oral environment. In implantology, it is used to condense bone substitutes, whether autologous, allogeneic, or synthetic, inside bone defects or around implants. This instrument also facilitates the placement of materials during sinus lifts or periodontal regenerations. Its use is strictly reserved for qualified healthcare professionals, ensuring an application in accordance with current clinical protocols for the reconstruction of bone volumes before or during implant placement.

What are the technical characteristics of this instrument?

On a technical level, this Hu-Friedy device belongs to the category of Class I durable consumables. Although exact material specifications are not detailed in the source data, the Black Line range is recognized for its dark coating that minimizes glare. The instrument is designed to offer an optimal grip during critical compaction phases. As a bone graft plugger, its geometry is adapted to reach narrow areas while allowing controlled pressure on the filling material. It meets the manufacturing standards of Hu-Friedy Mfg. Co., LLC, located in Chicago, ensuring compliance with regulatory requirements for Class I medical devices.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy, specific contraindications are not listed exhaustively outside of general warnings related to professional use. However, the use of this instrument is contraindicated for any person who does not have the qualification of a healthcare professional. It is imperative to refer to the instructions for use to identify any restrictions related to the patient's clinical state or incompatibilities with certain grafting materials. As with any oral surgery instrument, its use must be avoided if the instrument shows signs of wear or degradation that could compromise the safety of the surgical procedure.

What are the precautions for use and maintenance?

The Jovanovic Black Line plugger is a non-resorbable instrument that requires a strict cleaning and sterilization protocol between each patient. Although MDR data does not detail the reprocessing procedure, it is standard practice in dental surgery to follow the recommendations of the manufacturer Hu-Friedy to preserve the integrity of the Black Line coating. Practitioners must read the instructions carefully before use to ensure compliance with the recommended sterilization cycles. Careful handling is necessary to avoid damaging the working ends, which could alter precision during the condensation of materials during a bone graft.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, with headquarters located at 3232 N. Rockwell St. Chicago, Il 60618, USA. This medical device is classified as Class I according to current regulations. Compliance with manufacturing standards by Hu-Friedy ensures that the instrument meets safety and performance requirements for use in oral surgery. Although CE marking is not specifically mentioned in the source data, belonging to Class I indicates compliance with the classification rules for medical devices. Healthcare professionals must consult the attached technical documentation to guarantee use in accordance with the manufacturer's directives.

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Surgical medical consumables play a decisive role in operative safety.