Surgical Titanium Sinusline Cannula ⌀ 1.5mm - Helmut Zepf (19.651.13) - Delynov
The Canule chirurgicale Sinusline en titane ⌀ 1,5 mm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 19.651.13.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Helmut Zepf Sinusline surgical cannula?
The Sinusline surgical cannula (reference 19.651.13) is a specialized manual instrument developed by Helmut Zepf Medizintechnik GmbH. This device is distinguished by its titanium construction, a material of choice in surgical environments for its strength and lightness. Featuring a diameter of 1.5 mm, this titanium cannula is specifically sized for delicate interventions in the sinus area. It belongs to the category of reusable consumables after reprocessing. Its rigid structure allows for precise manipulation to maintain visibility of the surgical site by effectively evacuating fluids and debris during critical phases of oral surgery.
What are the clinical indications for this cannula?
This dental surgical cannula is primarily indicated for sinus surgery procedures, particularly sinus lift aspiration. It is used by implantologists and oral surgeons for sinus aspiration during the preparation of the bone window or the detachment of the Schneiderian membrane. Its 1.5 mm thinness makes it particularly useful for dental titanium aspiration in restricted spaces where standard cannulas would be too bulky. It facilitates the maintenance of a dry and clean surgical field, an essential condition for the success of bone grafts and implant placement in the posterior maxillary sector.
What are the technical characteristics of this device?
The Helmut Zepf Sinusline cannula features rigorous technical specifications to meet the requirements of oral surgery. It has a diameter of 1.5 mm, optimizing the ratio between suction flow and spatial footprint. Manufactured by Helmut Zepf Medizintechnik GmbH, it is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before the first use and between each patient. As a manual instrument, its titanium design guarantees excellent durability against thermal and chemical reprocessing cycles, while offering a biocompatible alternative for prolonged interventions in contact with soft and bone tissues.
What are the contraindications for the use of this instrument?
According to data from the manufacturer Helmut Zepf, the main contraindication is known patient intolerance to metals. Although titanium is highly biocompatible, any sign of hypersensitivity or intolerance reaction during contact with the instrument must lead to the immediate cessation of the procedure. Appropriate corrective measures must then be implemented. It is also contraindicated to use the product if it shows visible damage such as cracks, breaks, or structural defects. Use is strictly reserved for qualified healthcare professionals mastering sinus surgery techniques and asepsis protocols.
What are the maintenance and reprocessing precautions?
As it is a non-resorbable and reusable device, a strict reprocessing protocol is mandatory. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before each use. The practitioner must carefully inspect the cannula for any wear or damage before the procedure; the use of damaged products is prohibited. Due to its design and the materials used, there is no defined maximum limit for treatment cycles, but compatibility with other cleaning products must be verified beforehand. Rigorous internal cleaning is essential to guarantee the absence of biological residues in the lumen of the 1.5 mm cannula.
Who is the manufacturer and what standards are respected?
This cannula is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Germany. The device is classified as Class I (Class Ir according to the technical text) in accordance with medical device regulations. It meets the safety and performance requirements for manual dental instruments. The manufacturer emphasizes that safety of use depends on strict compliance with cleaning and sterilization instructions. As a Class I product, it benefits from German industrial rigor regarding surgical devices, ensuring practitioners a reliable tool for their daily interventions in implantology and periodontal surgery.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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