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

What is the Omnia 32.F2065 surgical aspiration line?

The Omnia surgical aspiration line, referenced under code 32.F2065, is a medical device designed for fluid evacuation during invasive procedures. This box of 10 units includes 2.20m long lines, each equipped with a sterile aspiration cannula and an adapter. Manufactured by Omnia S.p.A., this set is specifically structured to meet the requirements of sterility and reliability in a surgical environment. It maintains optimal visibility of the surgical site by efficiently suctioning blood and tissue debris, thus ensuring a clean working environment for the dental surgeon or implantologist.

What are the clinical indications for this aspiration set?

This surgical aspiration set is indicated for all oral surgery, implantology, and periodontology procedures requiring rigorous control of exudate and bleeding. Its use is particularly relevant during implant placement, sinus lifts, or complex extractions where field clarity is crucial. As a complete surgical aspirator, it integrates into the operating room preparation protocol to ensure constant suction. The device is intended exclusively for professional use by practitioners trained in surgical techniques, in accordance with the recommendations of the manufacturer Omnia S.R.L.

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

The Omnia sterile aspiration line features precise technical specifications to facilitate surgical movement. It measures 2.20m, a length adapted to move without tension between the patient and the suction unit. The kit includes a cannula and an adapter, allowing for broad compatibility with standard installations. This product belongs to Class I according to medical device regulations. The design by Omnia S.p.A. ensures fluid flow management without tube collapse, guaranteeing stable suction power throughout the operation, even during prolonged surgeries.

What are the contraindications for the use of this device?

According to the technical data provided by the manufacturer Omnia S.R.L., there are no specific medical contraindications listed for this 32.F2065 model other than those related to the general use of a suction system. However, the device is strictly reserved for qualified healthcare professionals. Inappropriate use or use by untrained personnel constitutes the main restriction of use. It is imperative to read the attached instructions carefully before use to ensure the equipment's compatibility with the specific clinical needs of the patient and the office equipment.

What are the precautions for use for this aspiration line?

As a Class I device marked CE1277, the handling of this surgical aspiration line must comply with standard aseptic protocols. Although the product is delivered for surgical use, the practitioner must check the integrity of the packaging before opening. As it is equipment intended for suction, care should be taken to ensure that no excessive bending obstructs the conduit during the procedure. After use, the device must be disposed of according to infectious clinical waste (DASRI) treatment protocols, in accordance with its nature as a single-use material to prevent any risk of cross-contamination.

Who is the manufacturer and what standards are respected?

The device is manufactured by Omnia S.p.A. (or Omnia S.R.L.), located in Fidenza, Italy. This product benefits from the CE1277 marking, certifying its compliance with European regulatory requirements for medical devices. Classified as Class I, this equipment meets the safety and performance standards required for dental surgery accessories. Omnia is a recognized manufacturer in the sector for the quality of its sterile devices. Healthcare professionals can refer to code 32.F2065 for the technical traceability of the product. The instructions for use must be consulted to comply with all manufacturer warnings.

State of the art

Single-use sterile surgical kits significantly reduce intraoperative contamination.