Universal raspatorium Helmut Zepf for (24.747.03) - Delynov

What is the Helmut Zepf universal periosteal elevator (24.747.03)?

The Helmut Zepf universal periosteal elevator, referenced under code 24.747.03, is a manual instrument specifically developed for oral surgery interventions. Manufactured in medical stainless steel by Helmut Zepf Medizintechnik GmbH, this device is designed to withstand the repeated sterilization cycles required in the practice. Its structure allows for rigorous tissue manipulation during bone exposure phases. As a decolleur instrument, it ensures effective separation of the periosteum. This device belongs to Class I of medical devices, guaranteeing its compliance with basic regulatory requirements for non-invasive or invasive instruments for temporary use.

What are the clinical indications for this surgical decolleur?

The primary indication for this manual dental instrument is the resection and elevation of soft tissues during various surgical procedures. In implantology, it is used to clear the bone site before drilling or implant placement. In periodontology, this surgical decolleur allows for the precise lifting of full-thickness flaps. It is also indicated for any intervention requiring the separation of the mucosa from the mineralized support, thus facilitating visibility and access to the surgical field. Its use is strictly reserved for qualified healthcare professionals mastering oral surgery techniques.

What are the technical characteristics of the 24.747.03 periosteal elevator?

The Helmut Zepf periosteal elevator (24.747.03) is characterized by its high-quality medical stainless steel manufacture. It is delivered non-sterile and must undergo a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient. Due to its robust design and the materials selected by Helmut Zepf Medizintechnik GmbH, there is no defined maximum limit for the number of processing cycles, although the instrument must be visually inspected before each use to detect any damage, cracks, or wear of the active parts.

What are the contraindications for the use of this instrument?

The main contraindication related to the use of this periosteal elevator is the patient's known hypersensitivity or intolerance to metals, particularly to the components of medical stainless steel. A hypersensitivity reaction can be triggered upon contact between the instrument and the tissues. The manufacturer specifies that if such a reaction occurs during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken accordingly. It is therefore recommended to check the patient's allergic history before any manipulation with this manual instrument.

What are the maintenance precautions to ensure safety?

Patient safety and instrument longevity depend on rigorous maintenance. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is crucial to inspect the instrument to identify visible damage, such as cracks, breaks, or defects on the cutting edges. The use of damaged or worn products is formally prohibited. Additionally, compatibility with other products used during the reprocessing chain must be verified beforehand to avoid any premature degradation of the stainless steel.

Who is the manufacturer and what standards are respected?

This device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. The universal periosteal elevator (24.747.03) is classified as a Class I medical device according to current regulations. The manufacturer imposes strict reprocessing protocols to maintain the compliance and safety of the instrument. As a Helmut Zepf product, it benefits from the expertise of a recognized manufacturer in the field of dental instrumentation, guaranteeing that the material used (medical stainless steel) meets the biocompatibility and resistance standards necessary for professional surgical practice.

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