Yankauer Model Canula - Omnia - Delynov (x10) - Delynov
The Canule modèle Yankauer - Omnia is a medical device manufactured by Omnia S.p.A. — Class I, CE marking CE1277.
- Compliance: Medical device Class I, CE marking CE1277.
- Manufacturer: Omnia S.p.A..
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Omnia Yankauer model cannula?
The Yankauer model cannula developed by Omnia is a single-use surgical instrument, specifically designed for aspiration needs in clinical environments. This device comes in the form of a rigid conduit intended to be connected to a centralized or mobile suction system. As a sterile yankauer cannula, it guarantees optimal microbiological safety for each patient, thus avoiding the risks of cross-contamination inherent in reusable devices. This consumable is packaged in boxes of 10 units to meet the needs of practices specialized in oral and maxillofacial surgery.
What are the clinical indications for this sterile surgical cannula?
The use of the yankauer cannula is indicated in numerous oral surgery procedures, notably during implant placement, management of periodontal flaps, or complex extractions. Its primary role is the continuous elimination of blood, saliva, and bone or tissue debris that can obstruct the visibility of the surgical site. By maintaining a clean intervention area, it allows the surgeon to operate with increased precision. It is particularly suitable for interventions requiring a constant suction flow and easy handling in posterior or difficult-to-access areas of the oral cavity.
What are the technical characteristics of this Omnia device?
The Yankauer model cannula produced by Omnia S.p.A. is designed to offer a stable grip and precise control of the suction flow. Although specific dimensions are not detailed, its design respects the ergonomic standards of classic Yankauer models used in hospital and dental office settings. This device belongs to the category of sterile consumables, ensuring immediate availability without the constraint of prior sterilization. Its structure is designed to avoid the attachment of soft tissues during aspiration, thus protecting the surrounding anatomical structures during the surgical gesture.
What are the contraindications for the use of the Yankauer cannula?
According to the technical documentation provided by the manufacturer Omnia S.p.A., there are no specific medical contraindications listed for the use of this cannula, outside of standard protocols related to surgical aspiration. However, the use of this device is strictly reserved for qualified healthcare professionals. It is imperative not to use the product if the sterile packaging is damaged, as the integrity of the sterile barrier would no longer be guaranteed. Practitioners must also ensure the compatibility of the connecting tubing with the diameter of the cannula to avoid any loss of suction power.
What are the precautions for use for this non-absorbable device?
As a non-absorbable and single-use device, the yankauer cannula must under no circumstances be cleaned, disinfected, or resterilized after a first use. Any attempt at reuse exposes the patient to serious infectious risks and can alter the mechanical properties of the material. After the intervention, the cannula must be disposed of in accordance with the disposal protocols for infectious clinical waste. The practitioner must carefully read the instructions for use provided by Omnia before any handling to ensure compliance with current safety and hygiene instructions.
Who is the manufacturer and what standards are respected?
The Yankauer model cannula is manufactured by Omnia S.p.A., an Italian company located in Fidenza, recognized for its expertise in the design of medical devices for surgery. This product is classified as a Class I medical device, meeting current safety and performance requirements. It carries the CE1277 marking, attesting to its compliance with European standards. Compliance with these regulations guarantees that the device has undergone the necessary controls for safe use during invasive surgical procedures. Traceability is ensured by the manufacturer for each lot produced.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
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