Diamond Points 2.35 mm for Helmut Zepf (31.185.12) - Delynov

What is the 31.185.12 diamond point for Helmut Zepf?

The 31.185.12 diamond point, distributed by Delynov, is a 2.35 mm rotary instrument designed by Helmut Zepf Medizintechnik GmbH. This device is specifically developed to meet the requirements of oral and dental surgery. Its structure incorporates a diamond coating on a medical stainless steel base, allowing for effective action on hard tissues. As a component of the CONSO category, this instrument is intended for strict professional use. Its design ensures compatibility with standard rotary systems accepting a shank diameter of 2.35 mm, thus ensuring smooth integration into the daily surgical workflow of dental practices and implantology centers.

What are the clinical indications for this instrument?

According to data from the manufacturer Helmut Zepf, this device is classified as a manual dental instrument intended for specific interventions in a clinical setting. In practice, this surgical diamond point is indicated for the preparation, remodeling, or rectification of hard tissues during various oral, periodontal, or implant surgery procedures. It is used by dental surgeons and implantologists for actions requiring controlled abrasion. Its use is reserved exclusively for qualified healthcare professionals trained in rotary surgery techniques. The instrument must be selected based on the specific needs of the procedure, taking into account the morphology of the area to be treated and the therapeutic objectives defined during surgical planning.

What are the technical characteristics of the diamond point?

The diamond point referenced under code 31.185.12 presents precise technical characteristics for surgery. It has a diameter of 2.35 mm, corresponding to the standards of surgical handpieces. Manufactured by Helmut Zepf Medizintechnik GmbH, it is composed of medical stainless steel, a material chosen for its mechanical resistance. The diamond coating ensures the abrasive function of the instrument. This product is delivered non-sterile, which requires a rigorous preparation protocol before any use. Before each intervention, the practitioner must imperatively inspect the instrument to detect any visible damage, such as cracks, breaks, or defects on the active parts. Any product showing signs of wear or degradation must be immediately discarded to guarantee the safety of care.

What are the contraindications for the use of this device?

The main contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Since the instrument is made of medical stainless steel, contact with the patient can trigger an allergic reaction in individuals sensitive to its components. If such a reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. Furthermore, the use of damaged or worn products is strictly prohibited, as it could compromise patient safety or the effectiveness of the surgical act. It is the practitioner's responsibility to check the patient's allergic history before any use of this rotary instrument in the mouth.

What are the maintenance and reprocessing 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 after each subsequent use. Prior cleaning is a critical step to remove any organic residue. Due to the design and materials used for this diamond point, the manufacturer specifies that it is not possible to define a maximum limit for treatment cycles. The lifespan of the instrument depends on the intended use and the actual wear observed by the professional. It is therefore essential to check the integrity of the instrument (absence of cracks or defects on the edges) before each sterilization cycle and before each surgical act to maintain an optimal performance level.

Who is the manufacturer and what standards are met?

This diamond point is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. The device is regulatory classified as Class I (Class Ir according to certain reprocessing nomenclatures). The manufacturer complies with the safety and performance requirements applicable to dental instruments. As a Class I medical device, it meets the rigorous quality standards imposed for reusable surgical instruments. Professionals can refer to the manufacturer's instructions for reprocessing and maintenance. Traceability is ensured by the technical reference 31.185.12, allowing for precise identification of the product within the Helmut Zepf range distributed by Delynov.

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Surgical medical consumables play a decisive role in operative safety.