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Burs - Helmut Zepf (12.300.02) - Delynov

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The fraises - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 12.300.02.
  • Reserved for healthcare professionals. Read instructions carefully before use.

133.63 € 133.63 EUR 133.63 € Tax Included

133.63 € Tax Included

(133.63 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf 12.300.02 bur?

The Helmut Zepf bur, referenced under code 12.300.02, is a manual dental instrument designed for oral surgery procedures. Manufactured by Helmut Zepf Medizintechnik GmbH, this instrument is crafted from high-quality medical stainless steel to ensure consistent performance during interventions. This device belongs to the category of consumables and is integrated into the standard surgical protocol of practitioners. Its structure is specifically studied to meet the requirements of healthcare professionals in clinical settings, offering a robust solution for the treatment of hard tissues. Like any instrument in this range, it requires expert handling and rigorous maintenance to maintain its cutting properties and longevity.

What are the clinical indications for this dental surgery bur?

The main indication for this instrument, as defined by the manufacturer Helmut Zepf Medizintechnik GmbH, is its use as a manual dental instrument. In clinical practice, this dental surgery bur is employed during various oral and implant surgery procedures. It allows the surgeon to perform precise cuts or adjustments on dental and bone structures. Its use is strictly reserved for qualified healthcare professionals. The intended purpose is to provide a reliable tool for interventions requiring controlled abrasion or sectioning, thus ensuring the smooth progress of the operative protocol while respecting the specific needs of each patient.

What are the technical characteristics of reference 12.300.02?

Technical reference 12.300.02 corresponds to a bur designed by Helmut Zepf. This device is classified as a Class I instrument according to current regulations. Its medical stainless steel composition gives it the necessary properties to withstand repeated cleaning and sterilization cycles, although the manufacturer specifies that a maximum limit of cycles cannot be defined in an absolute manner due to the variability of processing methods. Before each use, it is imperative to check for the absence of visible damage, such as cracks, breaks, or defects on the cutting edges, in order to guarantee the effectiveness of the instrument and the safety of the surgical act.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by the manufacturer concerns metal intolerance. Contact with this medical stainless steel instrument can cause a hypersensitivity reaction in certain sensitive patients. If such an allergic reaction or intolerance manifests during the intervention, the procedure must be stopped immediately and the necessary medical measures must be taken. It is therefore recommended to evaluate the patient's allergic history before any use. Furthermore, the use of the instrument is contraindicated if it shows visible signs of wear, cracks, or dull edges, as this could compromise the safety of the care.

What are the maintenance and sterilization precautions?

Helmut Zepf Medizintechnik GmbH products are delivered non-sterile. It is crucial to clean, disinfect, and sterilize each instrument before its first use, as well as after each subsequent use. The reprocessing process must be complete to ensure asepsis. The practitioner must carefully inspect the bur for any trace of wear or damage before each intervention. The use of damaged instruments is prohibited. Although the design and materials used do not allow for the definition of a maximum number of sterilization cycles, durability depends directly on compliance with cleaning protocols and systematic verification of the integrity of the cutting edges before each surgical act.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is listed under Class I (Class Ir according to certain reprocessing nomenclatures). The manufacturer complies with strict regulatory requirements for the design of manual dental instruments in stainless steel. As a Class I device, it meets the safety and performance standards applicable to this category of surgical instruments. Traceability and manufacturing quality are ensured by the expertise of Helmut Zepf, a recognized player in the field of dental instrumentation, thus guaranteeing healthcare professionals a product compliant with medical sector requirements.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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