Miller Double-Ended Bone File - Helmut Zepf (41.881.01) - Delynov

What is the Alveolotomy double Miller Bone File - Helmut Zepf (41.881.01)?

The double Miller Bone File for alveolotomy, referenced under code 41.881.01 by Helmut Zepf, is a high-precision manual dental instrument. Manufactured from medical stainless steel, this dental surgical file features a double configuration allowing for efficient handling during bone work. This device is specifically designed for oral surgery interventions requiring bone remodeling. As an instrument from the Helmut Zepf brand, it benefits from the expertise of Helmut Zepf Medizintechnik GmbH in specialized instrumentation for dental health professionals.

What are the clinical indications for this double bone file?

The double alveolotomy file is indicated for bone regularization procedures at the alveolar level. It is primarily used after tooth extraction to smooth sharp edges of the alveolar bone or during pre-implant surgeries to prepare the site. Its use allows for the elimination of bone irregularities that could compromise gingival healing or patient comfort under a prosthesis. This dental miller file is a tool of choice for dental surgeons and implantologists performing alveoloplasties or bone ridge corrections.

What are the technical characteristics of this instrument?

This instrument, identified by reference 41.881.01, is a double-sided miller bone file. Its medical stainless steel structure guarantees the necessary resistance to the stresses of bone surgery. It is a non-sterile device upon delivery, classified as Class I according to medical device regulations. The double design allows the practitioner to have two working ends to adapt to different areas of the dental arch without changing instruments, thus optimizing the operative flow during bone smoothing phases.

What are the contraindications for the use of the Helmut Zepf miller file?

The main contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity to the component materials. Metal intolerance in the patient may result from contact with the instrument, as it is manufactured from medical stainless steel. If a hypersensitivity reaction or an allergic reaction is triggered during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore crucial to check the patient's allergic history before any use.

What are the maintenance and sterilization precautions?

Like any reusable surgical instrument, this miller file must follow a strict reprocessing protocol. All instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. The manufacturer emphasizes the importance of checking for the absence of visible damage, such as cracks, breaks, or defects on the cutting edges, before each intervention. The use of damaged or worn products is prohibited. Due to the design and materials, there is no defined maximum limit of treatment cycles, but wear must be monitored by the professional.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik Gmbh, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I. In accordance with safety directives, the product is delivered non-sterile and must imperatively undergo a complete cleaning and sterilization cycle by the healthcare professional before use. The manufacturer specifies that the use of this instrument is strictly reserved for qualified healthcare professionals, thus ensuring an application compliant with current clinical protocols in dental and oral surgery.

State of the art

Surgical medical consumables play a decisive role in operative safety.