Kit de chirurgie Immediate Dentoalveolar Restoration (IDR) du Dr José Carlos Martins Da Rosa - Helmut Zepf (41.550.00) - Delynov

What is the Immediate Dentoalveolar Restoration (IDR) surgery kit?

The Immediate Dentoalveolar Restoration (IDR) surgery kit, referenced under code 41.550.00 at Delynov, is a set of specialized instruments designed by Helmut Zepf in collaboration with Dr. José Carlos Martins Da Rosa. This device belongs to the category of manual surgical instrumentation kits. Manufactured by Helmut Zepf Medizintechnik GmbH, it consists of instruments made of high-quality medical stainless steel. The structure of these tools is specifically designed to withstand the application of mechanical force via a hammer on the proximal part, transmitting energy to the sharp distal end to act on hard tissues. This equipment is delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use and between each patient.

What are the clinical indications for this kit?

The dental idr instrumentation is specifically indicated for immediate alveolar reconstruction procedures. According to data from the manufacturer Helmut Zepf Medizintechnik GmbH, the intended purpose is the use of a manual surgical instrument to cut or shape bone. In clinical practice, this dental idr kit is used during surgeries where the practitioner must harvest, reshape, or adapt bone grafts (often tuberosity grafts) to compensate for alveolar wall losses during immediate implantation. The technical gesture consists of striking the proximal end of the instrument with a hammer so that the distal cutting edge can sculpt the bone structure with precision. This alveolar surgery instrumentation is exclusively reserved for healthcare professionals trained in these complex protocols.

What are the technical characteristics of the instruments?

The instruments included in the IDR kit (reference 41.550.00) are classified as Class I medical devices. They are entirely manufactured from medical stainless steel, a material chosen for its mechanical resistance and its ability to withstand repeated sterilization cycles. The technical design is based on a force transmission axis: the proximal end is reinforced to receive impacts from a surgical hammer, while the distal end features a sharp or cutting edge sharpened for bone work. Helmut Zepf specifies that due to the nature of the materials used, there is no defined maximum limit for the number of processing cycles, as long as the physical integrity of the instrument is preserved. Each product must be visually inspected before use to detect any cracks or defects on the cutting edges.

What are the contraindications for using this equipment?

The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity to the material components. Metal intolerance in the patient may occur during contact with the medical stainless steel instrument. If a hypersensitivity reaction is triggered during the intervention, the procedure must be immediately interrupted and the necessary clinical measures must be taken. Furthermore, use is strictly contraindicated if the instrument shows visible damage, such as cracks, breaks, or defects on the sharp edges. The use of worn or damaged products compromises the safety of the surgical act and the integrity of the patient's tissues. Finally, this equipment must not be used by unqualified persons, as its use is strictly reserved for healthcare professionals.

What are the maintenance and sterilization precautions?

The Helmut Zepf IDR kit is delivered non-sterile. It is crucial to respect a strict reprocessing protocol before the first use and after each intervention. The instruments must be fully cleaned, disinfected, and sterilized in accordance with hospital hygiene standards. The manufacturer emphasizes the importance of thorough cleaning to remove any organic residue before the sterilization phase. Before each use, the practitioner must check compatibility with other products used and inspect the surface condition of the instruments. Any sign of premature wear or deformation must lead to the removal of the instrument from the clinical circuit. Although the design allows for many processing cycles, vigilance regarding the sharpness of the cutting edges is essential to maintain the effectiveness of the bone cutting.

Who is the manufacturer and what standards are met?

The IDR surgery kit is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer complies with regulatory requirements for medical devices, classifying this specific kit as Class I. As a reusable manual surgical device, it meets manufacturing standards in medical stainless steel to ensure the safety of patients and users. The instructions provided by Helmut Zepf Medizintechnik GmbH detail the responsibilities of the healthcare professional regarding the reprocessing and inspection of the equipment. Traceability is ensured by the product reference 41.550.00. It is reminded that the compliance of the device and the safety of the act depend on rigorous compliance with the cleaning and sterilization instructions issued by the manufacturer.

State of the art

Single-use sterile surgical kits significantly reduce intraoperative contamination.