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

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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.

30.06 € 30.06 EUR 30.06 € Tax Included 48.66 €

30.06 € Tax Included 48.66 €

(0.00 € / Units)
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Consumable

What is the Omnia Yankauer model cannula?

The Yankauer model cannula from the Omnia brand is a consumable medical device specifically designed for surgical suction procedures. This device features an ergonomic shape adapted to the needs of oral and maxillofacial surgery. Manufactured by Omnia S.p.A., this sterile yankauer cannula is delivered in individual packaging to guarantee total asepsis when introduced into the operative field. Its rigid structure allows for precise manipulation by the assistant or the practitioner, facilitating access to posterior or difficult-to-reach areas while ensuring a constant suction flow for the removal of biological fluids.

What are the clinical indications for this device?

Sterile yankauer suction is indicated for all oral surgery procedures requiring rigorous control of exudate, blood, and irrigation solutions. In implantology, it is used to clear the drilling site and ensure a clear vision during implant placement. In periodontal surgery, it allows for the efficient elimination of fluids during full-thickness flaps or bone grafts. Its use is also relevant during complex extractions or soft tissue surgery, where the accumulation of liquids can hinder the precision of the surgical gesture. This Omnia device meets the microbiological cleanliness requirements essential in a sterile environment.

What are the technical characteristics of the yankauer cannula?

The sterile yankauer cannula developed by Omnia S.p.A. is characterized by a robust design suitable for professional use in dental offices or operating rooms. Although specific dimensions are not detailed, the Yankauer model is recognized for its rounded tip and lateral orifices that prevent accidental suction of surrounding soft tissues, thus minimizing interruptions during the technical procedure. As a Class I consumable, it complies with European manufacturing standards for non-invasive or short-term invasive medical devices. Its standard connection allows for rapid adaptation to the majority of surgical suction units on the market.

What are the contraindications for the use of this device?

According to the data provided by the manufacturer Omnia S.p.A., there are no specific clinical contraindications listed for the use of this suction cannula, other than those related to standard surgical protocols. 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, in order to avoid any risk of cross-contamination. The practitioner must ensure that the suction technique employed is adapted to the fragility of the tissues concerned and the type of procedure performed. The instructions for use must be carefully consulted before any manipulation to comply with safety instructions.

What are the precautions for use for this sterile cannula?

The Omnia sterile yankauer cannula is a single-use device. Consequently, it must not be cleaned, resterilized, or reused after an initial procedure, as this could compromise patient safety and suction efficiency. Maintaining sterility until the moment of use is crucial to prevent post-operative infections. After use, the cannula must be disposed of in accordance with the disposal protocols for infectious clinical waste. The practitioner must ensure that the connection with the suction tube is airtight to guarantee optimal sterile yankauer suction power throughout the surgical procedure.

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 surgical medical devices. This product carries the CE1277 marking, certifying its compliance with the safety and performance requirements defined by European regulations. It is classified as a Class I medical device. Compliance with these standards guarantees dental surgeons and implantologists a reliable, controlled product adapted to the constraints of the modern surgical environment. Traceability is ensured by the manufacturer Omnia S.R.L., in accordance with the directives in force for medical devices intended for healthcare professionals.


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Surgical medical consumables play a decisive role in operative safety.

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