Suction Tip Frazier Canula (19.641.03) - Delynov

What is the Helmut Zepf Frazier Suction Cannula?

The Helmut Zepf Frazier Suction Cannula, referenced under code 19.641.03, is a manual instrument designed for fluid management in surgical settings. Manufactured by Helmut Zepf Medizintechnik GmbH, this dental surgery suction cannula is crafted from high-quality medical stainless steel. It features a thin tubular structure with a 3mm diameter, adapted to the specific needs of localized aspiration. This device belongs to the category of reusable consumables, requiring a strict cleaning and sterilization protocol before each use. Its design allows for precise manipulation to clear the operative field without obstructing the practitioner's workspace.

What are the clinical indications?

This frazier cannula is indicated for all oral surgery, implantology, and periodontology procedures requiring meticulous aspiration. It is particularly useful during osteotomies, complex extractions, or sinus lifts where visual field clarity is critical. As a manual dental instrument, it effectively removes biological fluids and irrigation residues. Its use is exclusively reserved for qualified healthcare professionals, ensuring safe application in compliance with clinical protocols in force in dental practices and oral surgery centers.

What are the technical characteristics?

The Helmut Zepf Frazier suction cannula (ref. 19.641.03) is distinguished by a 3mm diameter, offering an ideal compromise between suction flow and access fineness. It is manufactured from medical stainless steel, a material chosen for its resistance to repeated sterilization cycles. The device is delivered non-sterile and must undergo complete processing (cleaning, disinfection, and sterilization) before its first use. Its ergonomic design meets the requirements of surgeons performing long-duration interventions, ensuring frazier suction stability throughout the operative act.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns patients with known hypersensitivity or intolerance to metals, specifically the medical stainless steel used to manufacture the instrument. An allergic reaction may be triggered upon contact with the mucosa or tissues. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore recommended to check the patient's allergic history before any use of this surgical instrument.

What are the maintenance and safety precautions?

All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is crucial to visually inspect the cannula before each intervention to detect potential damage such as cracks, breaks, or surface defects. The use of damaged or worn products is strictly prohibited. Due to its design and the materials used, there is no defined maximum limit for processing cycles, but visible wear must lead to the removal of the device. Compatibility with other products used simultaneously must also be verified beforehand by the practitioner.

Who is the manufacturer and what standards are respected?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Germany. The product is classified as a Class I medical device according to current regulations. It meets the quality requirements for medical stainless steel to ensure the safety of patients and users. As a Class I device, it follows the conformity assessment procedures applicable to this category of manual non-invasive or short-term invasive instruments. Compliance with the reprocessing instructions provided by Helmut Zepf is essential to maintain the integrity of the device and clinical safety during each surgical act.

State of the art

Surgical medical consumables play a decisive role in operative safety.