Surgical Vacuum Cleaner Sinusline - Helmut Zepf (19.651.30) - Delynov
The Aspirateur chirurgical Sinusline - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.
- Compliance: Medical device Class I.
- Manufacturer: Helmut Zepf Medizintechnik GmbH.
- Reference: 19.651.30.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Sinusline Helmut Zepf surgical aspirator?
The Sinusline surgical aspirator, bearing reference 19.651.30, is a manual instrument developed by Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, this device is specifically designed to meet the requirements of oral surgery. As a dental surgery aspirator, it comes in the form of an ergonomic cannula allowing for targeted aspiration. This equipment is delivered non-sterile and requires a complete protocol of cleaning, disinfection, and sterilization before its first use and between each patient. Its robust stainless steel design ensures compatibility with standard thermal and chemical reprocessing cycles in dental practices.
What are the clinical indications for this instrument?
This dental surgical aspirator is primarily indicated for oral surgery interventions, particularly during sinus lift or sinus floor elevation protocols. The Sinusline sinus aspiration cannula allows the practitioner to effectively eliminate blood, saliva, and bone debris without obstructing the vision of delicate anatomical structures. Its use is essential to guarantee the clarity of the operative site during the preparation of the bony window or the detachment of the Schneiderian membrane. It integrates perfectly into the workflow of dental surgeons and implantologists performing sub-sinus bone augmentations.
What are the technical characteristics of reference 19.651.30?
The Sinusline Helmut Zepf aspirator (reference 19.651.30) is distinguished by its manufacture in high-quality medical stainless steel. Categorized as a Class I device, this instrument is designed for prolonged durability despite repeated sterilization cycles. Its geometry is specifically adapted to access the posterior areas of the maxilla, thus facilitating the use of the surgical cannula in restricted spaces. Helmut Zepf has not defined a maximum limit for treatment cycles, as longevity depends on maintenance and the absence of visible damage such as cracks or breaks during pre-operative inspection.
What are the contraindications for the use of this aspirator?
The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns known hypersensitivity or metal intolerance. Since the instrument is composed of medical stainless steel, contact with the patient can trigger an allergic reaction in sensitive individuals. If a hypersensitivity reaction occurs during the intervention, the procedure must be immediately interrupted and appropriate medical measures must be initiated. It is therefore imperative to check the patient's allergic history before any use of this manual instrument in the mouth.
What are the maintenance and reprocessing precautions?
As it is a non-resorbable and reusable instrument, compliance with safety instructions is paramount. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The practitioner must imperatively inspect the product to detect any visible damage, such as cracks, breaks, or surface defects. The use of damaged or worn products is strictly prohibited. Compatibility with other aspiration devices must also be verified beforehand to guarantee the seal and efficiency of the surgical aspiration system during the operative act.
Who is the manufacturer and what standards are met?
The Sinusline aspirator is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer emphasizes that its products are exclusively reserved for qualified healthcare professionals. Compliance with safety standards relies on a rigorous reprocessing protocol including systematic cleaning and sterilization. As a Class I device, it meets the safety and performance requirements for reusable manual stainless steel dental instruments.
State of the art
Surgical medical consumables play a decisive role in operative safety.
Specifications
| Manufacturer | Helmut Zepf |
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