Oral Surgery and Implantology Probe Helmut Zepf (24.102.23) - Delynov

What is the Helmut Zepf (24.102.23) oral surgery probe?

The Helmut Zepf oral surgery and implantology probe, referenced under code 24.102.23, is a manual instrument designed specifically for interventions in the oral environment. Manufactured by Helmut Zepf Medizintechnik GmbH, this probe is developed from high-quality medical stainless steel to guarantee optimal resistance during clinical manipulations. As a Class I device, it meets the regulatory requirements for non-invasive or short-term invasive instruments. Its structure is designed to offer direct and precise handling, essential for intraoperative diagnostics in dental surgery.

What are the clinical indications for this instrument?

This probe is primarily indicated for oral surgery and implantology. Its use is recommended for tissue exploration, verifying drilling depths, or examining alveolar structures. It integrates perfectly into dental surgery protocols where precise tactile and visual evaluation is required. The instrument allows for the identification of bony reliefs and ensures site compliance before the insertion of implantable devices. Its role is fundamental for securing the surgical procedure by providing the practitioner with immediate topographical information on the treated area.

What are the technical characteristics of the 24.102.23 probe?

The Helmut Zepf probe is distinguished by its manufacture in medical stainless steel, a material chosen for its biocompatibility and its ability to undergo repeated sterilization cycles. Although delivered non-sterile, it is designed to withstand the mandatory cleaning, disinfection, and sterilization protocols before any use. The technical reference 24.102.23 corresponds to a specific configuration adapted to the needs of modern implantology. Its ergonomic design allows for a stable grip, facilitating delicate measurements in difficult-to-access areas of the oral cavity.

What are the contraindications for the use of this probe?

The main medical contraindication lies in the patient's known hypersensitivity or intolerance to metals, particularly the medical stainless steel used in the instrument's composition. If a hypersensitivity reaction occurs during the procedure, the process must be immediately interrupted and appropriate clinical measures must be taken. It is also forbidden to use the instrument if it shows visible damage such as cracks, breaks, or defects on the active parts, as this could compromise patient safety or the precision of the procedure.

What are the maintenance and reprocessing precautions?

Helmut Zepf Medizintechnik GmbH products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as between each patient. Thorough cleaning is crucial to remove any residue before the sterilization cycle. The practitioner must inspect the instrument for any visible wear before use. Due to the robust design and materials used, there is no defined maximum limit of treatment cycles, as long as the physical integrity of the probe is preserved. Use is strictly reserved for qualified healthcare professionals.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer imposes strict reprocessing protocols to guarantee clinical safety. Compliance with medical stainless steel standards ensures that the instrument meets the durability and safety requirements necessary in a surgical environment. Each probe is identified by a unique reference (24.102.23) allowing for precise traceability within the dental office or clinic.

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