Suction Cannula ⌀ 3 mm - Helmut Zepf (19.649.30) - Delynov

What is the ⌀ 3 mm suction cannula - Helmut Zepf?

The ⌀ 3 mm suction cannula from the brand Helmut Zepf is a precision surgical instrument designed for the operating room. Manufactured by Helmut Zepf Medizintechnik GmbH, this cannula (reference 19.649.30) is made of medical stainless steel, a standard material for reusable instrumentation. It is a rigid tubular device allowing for effective surgical aspiration of fluids and debris. This device belongs to Class I of medical devices. Its structure is optimized to meet the sterility and durability requirements necessary in a clinical setting, although it is delivered non-sterile by the manufacturer.

What are the clinical indications?

Surgical aspiration using this 3 mm cannula is indicated for the active cleaning of the surgical field. It is used for periodic or continuous aspiration of body cavities or wounds during an intervention. In oral or implant surgery, it allows for the removal of loose tissues, blood, saliva, and other fluid residues. The clinical objective is to maintain a clear surgical field to improve the practitioner's visibility and facilitate access to intervention areas, thus ensuring better precision during complex surgical maneuvers.

What are the technical characteristics?

This Helmut Zepf suction cannula has an internal diameter of 3 mm, a dimension adapted to common needs in oral surgery. Listed under code 19.649.30, it is designed to be compatible with standard operating room suction systems. Its medical stainless steel construction allows it to withstand repeated cleaning and sterilization cycles. As a Class I device, it meets regulatory safety requirements. Its rigid design ensures precise handling by the assistant or surgeon, preventing any deformation when aspirating denser residues.

What are the contraindications for use?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity to the constituent materials. Metal intolerance, particularly to components of medical stainless steel, can trigger a hypersensitivity reaction in certain patients upon contact with the instrument. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore crucial to check the patient's allergic history before any use of metallic instrumentation.

What are the maintenance and reprocessing precautions?

Helmut Zepf products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as between each patient. It is essential to visually inspect the cannula for any damage such as cracks, breaks, or defects on the edges before use. A damaged or worn instrument must never be used. Due to its stainless steel design, there is no defined maximum limit for processing cycles, but compatibility with other cleaning products must be verified beforehand by the healthcare professional.

Who is the manufacturer and what standards are met?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This device is classified as a Class I instrument according to current regulations. Compliance with cleaning and sterilization protocols is the responsibility of the healthcare professional, in accordance with the instructions provided by Helmut Zepf. The product is strictly reserved for professional use in a surgical environment. Traceability is ensured by the technical reference 19.649.30, guaranteeing the origin and compliance of the equipment with the German company's manufacturing standards.

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Surgical medical consumables play a decisive role in operative safety.