1 box of 10 surgical suction lines 2.20m with cannula (with adapter) (32.F2065) - Omnia - Delynov

What is the box of 10 Omnia surgical suction lines?

This box contains 10 surgical suction lines from the brand Omnia, specifically designed for dental procedures. Each line measures 2.20m in length and is equipped with a cannula and an adapter. This medical device, identified under reference 32.F2065, is presented as a ready-to-use set for the practitioner. The surgical aspirator is an essential element of the technical platform, allowing for optimal visibility during operative acts. This lot of 10 units allows for efficient stock management for clinics regularly practicing oral surgery or implantology. The product is manufactured by Omnia S.p.A., guaranteeing recognized expertise in the field of sterile single-use devices.

What are the clinical indications for this suction device?

The intended use for these Omnia suction lines concerns the aspiration of oral fluids and residues during surgical interventions. This device is indicated for surgical suction in a dental environment, where fluid management is critical to the success of the procedure. It is used via a mobile suction unit to effectively evacuate blood, saliva, and tissue or bone debris. This equipment is strictly reserved for qualified healthcare professionals, such as dental surgeons, stomatologists, or implantologists. Its use helps secure the operative field by ensuring constant and precise evacuation of disruptive elements throughout the duration of the intervention.

What are the technical characteristics of the 32.F2065 suction line?

The Omnia surgical suction line features precise technical specifications to meet the requirements of the dental operating suite. It has a length of 2.20m, offering sufficient freedom of movement between the mobile suction unit and the operative field. The kit includes a cannula and an adapter, facilitating connection and handling during suction. This product is categorized as a Class IIa medical device according to current regulations. Reference 32.F2065 corresponds to a quality standard for surgical suction procedures. The cannula design is optimized to reach difficult access areas while guaranteeing a constant and efficient suction flow for the removal of fluids and residues.

What are the contraindications and limitations for the use of this equipment?

Although the source data does not list specific contraindications related to materials, the use of this device is strictly limited to the dental surgical indications for which it was designed. It must not be used outside of the professional healthcare setting. Improper handling or an unsuitable connection to the mobile suction unit could compromise suction efficiency. It is imperative not to use the product if the packaging is damaged, in order to guarantee the asepsis of the operative field. As this device is single-use, any attempt at reprocessing or reuse is prohibited to avoid risks of cross-contamination between patients. Practitioners should refer to the instructions for use for any additional warnings.

What are the precautions for use for surgical suction?

To guarantee efficient and safe suction, the healthcare professional must read the instructions carefully before any use. It is crucial to verify the compatibility between the Omnia line adapter and the mobile suction unit used in the clinic. During the intervention, the cannula must be handled with precision to avoid any trauma to the surrounding soft tissues. The 2.20m length must be managed so as not to hinder the movements of the surgical team while avoiding kinks that could block the suction flow. After the intervention, the entire line and cannula must be disposed of according to the protocols for managing infectious clinical waste (DASRI), in accordance with good hospital hygiene practices.

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

These surgical suction lines are manufactured by the official manufacturer Omnia S.p.A., a company specializing in medical devices for dental surgery. The product complies with medical device regulations and is categorized as Class IIa. This classification certifies that the device meets strict safety and performance requirements for its intended use in a surgical environment. Traceability is ensured by the manufacturer, and each box of 10 units allows for rigorous tracking of the lots used in the clinic. Compliance with these standards guarantees dental surgeons the use of reliable equipment for the suction of fluids and residues during their most demanding operative acts.

State of the art

Single-use sterile surgical kits significantly reduce intraoperative contamination.