Osteotome Set I - Helmut Zepf (47.949.90) - Delynov

What is the Helmut Zepf osteotome set I?

The Helmut Zepf osteotome set I (reference 47.949.90) is a high-quality manual dental instrument manufactured by Helmut Zepf Medizintechnik GmbH. Designed in medical stainless steel, this device is specifically developed to meet the requirements of bone surgery. This osteotome kit is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient. As a Class I medical device, it is part of the arsenal of precision instruments intended for healthcare professionals practicing implantology and oral surgery.

What are the clinical indications for this surgical osteotome kit?

This implantology osteotome set is indicated for oral surgery procedures requiring precise manipulation of bone structures. Its main use concerns the preparation of the implant site, particularly for the condensation of cancellous bone or the elevation of the sinus floor during a sinus lift osteotome kit procedure. The instrument allows for optimizing local bone density and preparing the socket in a controlled manner. It is exclusively reserved for use by qualified healthcare professionals, thus guaranteeing an application in accordance with current clinical standards in implantology.

What are the technical characteristics of this instrument?

The Helmut Zepf osteotome set I, bearing technical reference 47.949.90, is manufactured from medical stainless steel selected for its resistance and compatibility with reprocessing cycles. The manufacturer, Helmut Zepf Medizintechnik GmbH, specifies that due to the robust design and materials used, there is no defined maximum limit for the number of achievable processing cycles, as long as the instrument does not show visible damage. It is imperative to check for the absence of cracks, breaks, or defects on the cutting edges before each intervention to ensure surgical safety.

What are the contraindications for the use of these dental osteotomes?

The main contraindication for the use of this instrument is the patient's known intolerance or hypersensitivity to metals, particularly medical stainless steel. A hypersensitivity reaction can be triggered upon contact with the instrument. If such a reaction occurs during the surgical act, the manufacturer Helmut Zepf stipulates that the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore crucial to evaluate the patient's allergic history before any use of this equipment in the mouth.

What are the maintenance and reprocessing precautions?

All instruments in the surgical osteotome kit must imperatively be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The manufacturer emphasizes the vital importance of cleaning to remove all residue before sterilization. Before each use, the practitioner must meticulously inspect the instrument to detect any visible damage or wear such as cracks or breaks. The use of damaged or worn products is strictly prohibited. Compatibility with other products used simultaneously must also be verified beforehand by the professional.

Who is the manufacturer and what standards are respected?

The osteotome set I is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer ensures the traceability and compliance of its manual dental instruments intended for dental surgery experts. Compliance with the cleaning and sterilization protocols described by the manufacturer is essential to maintain the device's conformity throughout its useful life. This professional equipment meets strict manufacturing requirements for reusable invasive surgical devices.

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