Yankauer Model Canula - Omnia - Delynov (x10) - Delynov

What is the Omnia Yankauer model cannula?

The Yankauer model cannula developed by Omnia is a consumable medical device specifically designed for fluid aspiration in a surgical environment. This device features an ergonomic shape adapted to the needs of practitioners performing interventions in the oral cavity. As a sterile yankauer cannula, it guarantees rigorous hygiene for each patient, avoiding the risks of cross-contamination inherent in reusable devices. Its structure allows for easy handling to reach difficult access areas during complex oral surgeries. This Omnia product is delivered in packs of 10 units, meeting the logistical requirements of dental practices and implantology centers.

What are the clinical indications for this suction cannula?

The use of the yankauer suction cannula is indicated in numerous oral surgery procedures, notably during implant placement, bone grafting, or periodontal surgery. Its primary role is to ensure effective sterile yankauer suction of blood, saliva, and tissue or bone debris generated during the operative act. Maintaining optimal visibility of the intervention site is crucial for surgical precision, particularly during implant drilling or flap suturing. Although specific MDR indications are not detailed in the technical documentation provided, the standard use of this type of device concerns perioperative fluid management by healthcare professionals.

What are the technical characteristics of this device?

The Yankauer model cannula manufactured by Omnia S.p.A. is distinguished by its compliance with European safety standards. This medical device is classified as Class I, which corresponds to products presenting a low degree of risk according to current regulations. It bears the CE1277 marking, certifying its compliance with the health and safety requirements defined by the notified body. Although exact dimensions or specific materials are not listed in the source data, the design is optimized to fit standard suction systems used in dental practices. Each cannula is intended for single use to ensure total microbiological safety during each surgical intervention.

What are the contraindications for the use of the Yankauer cannula?

According to the information provided by the manufacturer Omnia S.p.A., there are no specific medical contraindications listed for this device. However, the use of this cannula is strictly reserved for qualified healthcare professionals. It is imperative to read the instructions for use carefully before any handling. As with any sterile device, use is contraindicated if the individual packaging is damaged or open, as the integrity of the sterile barrier would no longer be guaranteed. The practitioner must evaluate the compatibility of the device with the patient, although no particular intolerance is reported in the manufacturer's raw technical documentation.

What are the precautions for use and handling?

The sterile yankauer cannula must be handled with care to maintain its aseptic state until the operative site. As a non-resorbable and non-implantable device in the surgical sense of the term, precautions mainly concern the management of medical waste after use. The product is for single use and must under no circumstances be resterilized or reused, at the risk of losing its functional properties and risking a nosocomial infection. The practitioner must ensure that the cannula is correctly connected to the centralized or portable suction system of the practice before starting the intervention. Visual monitoring of the suction flow is recommended to avoid any obstruction by large debris during surgery.

Who is the manufacturer and what standards are respected?

The Yankauer model cannula is manufactured by Omnia S.p.A., a recognized Italian company located in Fidenza. The manufacturer respects rigorous quality protocols for the production of its medical devices. This product benefits from the CE1277 marking, guaranteeing its compliance with the European directives applicable to Class I devices. Traceability and safety are at the heart of Omnia's manufacturing process, ensuring dental surgeons and implantologists a reliable equipment for their operating rooms. As a Class I medical device, it meets the essential safety and performance requirements for professional use in a controlled clinical environment.

State of the art

Surgical medical consumables play a decisive role in operative safety.