Syringe water for dental surgery - Helmut Zepf (19.762.00) - Delynov

What is the Helmut Zepf water syringe cannula?

The Helmut Zepf water syringe cannula, referenced under code 19.762.00, is a manual dental instrument designed to be adapted to irrigation syringes. Manufactured in medical stainless steel by Helmut Zepf Medizintechnik GmbH, it is specifically structured to allow controlled projection of water or rinsing solutions into the oral cavity. This device belongs to the consumables category (CONSO) and is classified as a Class I medical device. Its robust metal design ensures compatibility with the rigorous thermal and chemical reprocessing protocols required in dental practices.

What are the clinical indications for this tip?

This dental syringe cannula is indicated for all procedures requiring precise irrigation of the operative site. In oral surgery, it facilitates the removal of debris, blood, or milling residues, thereby offering better visibility to the practitioner. It is commonly used during socket cleaning phases after extraction or for rinsing periodontal pockets. Its use is strictly reserved for qualified healthcare professionals, guaranteeing safe handling adapted to the clinical needs of implantology and restorative dentistry.

What are the technical characteristics of the 19.762.00 cannula?

The Helmut Zepf water syringe cannula is distinguished by its high-quality medical stainless steel manufacturing. Although delivered non-sterile, it is designed to withstand repeated cycles of cleaning, disinfection, and sterilization without alteration of its mechanical properties. The manufacturer, Helmut Zepf Medizintechnik GmbH, does not define a maximum limit for treatment cycles, as the lifespan depends on maintenance and the absence of visible damage. It is imperative to check for the absence of cracks, breaks, or defects before each use to ensure patient safety.

What are the contraindications for the use of this device?

The main contraindication mentioned by the manufacturer concerns hypersensitivity or metal intolerance. As the instrument is composed of medical stainless steel, contact with the patient can trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. Furthermore, it is strictly forbidden to use a cannula showing visible signs of wear, cracks, or deformations that could compromise its integrity or the safety of care.

What are the maintenance and sterilization precautions?

Helmut Zepf products are delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before the first use, as well as between each patient. Reprocessing must follow the standard protocols in force for stainless steel instruments. Before each use, the practitioner must carefully inspect the cannula to detect any damage such as cracks or defects on the edges. The use of damaged or worn products is prohibited. Compatibility with other syringe devices must also be verified prior to the clinical act.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This product is a Class I instrument compliant with the regulatory requirements applicable to non-invasive or invasive medical devices for temporary use. Compliance with manufacturing protocols and the choice of medical stainless steel ensure compliance with safety standards for use in a surgical environment. As a Helmut Zepf product, this cannula benefits from the expertise of a company specialized in precision instrumentation for dental and maxillofacial surgery.

State of the art

Surgical medical consumables play a decisive role in operative safety.