Bands for Matrix for Dental Surgery and Implantology - Helmut Zepf (19.061.02) - Delynov

What is the Helmut Zepf 19.061.02 matrix band?

The Helmut Zepf matrix band (reference 19.061.02) is a Class I medical device designed for dental surgery and implantology procedures. This stainless steel matrix band is manufactured from high-quality medical stainless steel, ensuring mechanical resistance adapted to the constraints of the oral cavity. As a manual dental instrument, it is used to surround the tooth during restorations to compensate for the absence of a dental wall. This device is delivered non-sterile by Helmut Zepf Medizintechnik GmbH and requires a full cycle of cleaning, disinfection, and sterilization before each use to guarantee the safety of the patient and the practitioner.

What are the clinical indications for this dental surgery matrix?

This dental surgery matrix is indicated for the restoration of Class II, III, and IV cavities according to Black's classification, as well as for pre-implant reconstruction procedures requiring temporary formwork. It allows for the confinement of restorative materials, ensures an optimal contact point with adjacent teeth, and prevents material overflow into the gingival sulcus. The use of this steel matrix band is exclusively reserved for qualified healthcare professionals, such as dental surgeons and implantologists, operating in a controlled clinical environment.

What are the technical characteristics of this steel matrix band?

The matrix band referenced 19.061.02 is characterized by its medical stainless steel composition, a material chosen for its biocompatibility and its ability to undergo repeated sterilization cycles without alteration of its physical properties. Its design allows for precise adaptation to the cervical and proximal contours of the dentition. Helmut Zepf Medizintechnik GmbH emphasizes that, although no maximum limit for processing cycles is defined by the design, the instrument must be visually inspected before each use to detect any damage such as cracks, breaks, or defects on the cutting edges.

What are the contraindications for the use of this device?

The main contraindication for the use of this Helmut Zepf device is known hypersensitivity or intolerance of the patient to metals, specifically medical stainless steel. An allergic reaction may be triggered upon contact between the instrument and the mucosal tissues. If such a hypersensitivity reaction occurs during the procedure, the manufacturer stipulates that the intervention must be immediately stopped and necessary medical measures must be taken. It is therefore imperative to check the patient's allergic history before any clinical application.

What are the maintenance and reprocessing precautions?

As this stainless steel matrix band is non-resorbable and intended for temporary intraoperative use, it must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. Helmut Zepf products are delivered non-sterile. The practitioner must check for the absence of visible damage such as cracks or defective cutting edges before use. The use of damaged or worn products is strictly prohibited. Compatibility with other products used during surgery must also be verified beforehand to avoid any undesirable interaction.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This matrix band is classified as a Class I medical device according to current regulations. The manufacturer respects rigorous manufacturing protocols for manual instruments in medical stainless steel. The reprocessing process must follow the manufacturer's safety instructions to maintain product compliance. This device is exclusively intended to be handled by healthcare professionals trained in dental surgery and implantology techniques.

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