Surgical cannula Sinusline ⌀ 1.5mm in titanium - Helmut Zepf (19.651.15) - Delynov

What is the Sinusline ⌀ 1.5mm cannula?

The Sinusline ⌀ 1.5mm cannula is a specialized instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed to meet the requirements of oral surgery, this titanium surgical cannula is distinguished by its titanium composition and its fine diameter of 1.5mm. Unlike standard instruments, its structure is adapted to surgical environments requiring precise fluid management. It belongs to the category of reusable consumables (CONSO) and is identified under the technical reference 19.651.15. Its design allows for easy handling by the practitioner during critical phases of the intervention.

What are the clinical indications for this cannula?

This cannula is primarily indicated for dental sinus aspiration. In implant and oral surgery, it facilitates the maintenance of a clear operative field during sinus lifts or during the preparation of implant sites. Its use is reserved for qualified healthcare professionals. It is particularly useful for dental surgery aspiration in areas where space is restricted, allowing for the effective removal of blood, saliva, or bone debris without obstructing the surgeon's visibility of sensitive anatomical structures.

What are the technical characteristics of this device?

The Sinusline cannula referenced 19.651.15 has a diameter of 1.5mm, making it a high-precision tool. Manufactured by Helmut Zepf, it uses titanium as the primary material, offering specific properties for surgical instrumentation. This device is classified as a Class I manual dental instrument according to current regulations. It is delivered non-sterile and requires a complete processing protocol before each use. Its design allows it to withstand cleaning, disinfection, and sterilization cycles, although no maximum limit of cycles is defined by the manufacturer due to the nature of the materials used.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns metal intolerance in the patient. Contact with the instrument can trigger a hypersensitivity reaction. If such a reaction occurs during the intervention, the procedure must be immediately stopped and the necessary clinical measures must be taken. Furthermore, it is strictly forbidden to use products showing visible damage or wear, such as cracks, breaks, or defects on the edges, to guarantee patient safety and the effectiveness of the surgical gesture.

What are the maintenance and reprocessing precautions?

All Helmut Zepf instruments must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. Cleaning must be complete and thorough to remove all residues. Before each use, the practitioner must check for the absence of visible damage. As the products are delivered non-sterile, compliance with sterilization protocols is crucial. Due to the robust design and selected materials, there is no defined maximum limit for treatment cycles, but compatibility with other products used simultaneously must be verified beforehand by the 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 medical device complies with Class I (Class Ir according to certain reprocessing nomenclatures). As a manual dental instrument, it meets the safety and performance requirements defined for its category. The manufacturer emphasizes that the use of these instruments is strictly reserved for healthcare professionals. Following safety instructions, particularly regarding cleaning and wear verification, is essential to maintain compliance and safety of use within the dental office or clinic.

State of the art

Surgical medical consumables play a decisive role in operative safety.