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Plate Plier based on Dr. Dirk Brozio - Helmut Zepf (22.107.21) - Delynov

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The Pince Plate d'après Dr. Dirk Brozio - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 22.107.21.
  • Reserved for healthcare professionals. Read instructions carefully before use.

117.99 € 117.99 EUR 117.99 € Tax Included

117.99 € Tax Included

(117.99 € / Units)
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Instrument

What are the flat pliers according to Dr. Dirk Brozio?

The flat pliers according to Dr. Dirk Brozio, referenced under code 22.107.21 at Delynov, are a manual instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, these technical flat pliers are specifically adapted to the requirements of oral surgery and guided bone regeneration (GBR). Their structure is designed to offer a reliable grip during delicate manipulations in a clinical setting. As an instrument from the Helmut Zepf brand, it benefits from the expertise of a recognized manufacturer in the field of high-precision dental instrumentation.

What are the clinical indications for these flat dental pliers?

These flat dental pliers are indicated as a manual instrument for dental surgery interventions, particularly in bone regeneration protocols. They are primarily used by dental surgeons and implantologists for handling devices or materials necessary for tissue reconstruction. Their use is strictly reserved for qualified healthcare professionals. They are integrated into surgical procedures requiring surgical flat pliers to hold or position elements with stability, in accordance with the operating techniques recommended by Dr. Dirk Brozio.

What are the technical characteristics of the 22.107.21 pliers?

The Helmut Zepf dental surgery flat pliers (reference 22.107.21) are designed in medical grade stainless steel, guaranteeing resistance to repeated cleaning and sterilization processes. This is a Class I device. Although there is no defined maximum limit for the number of processing cycles due to the robustness of the materials used, the instrument must be inspected before each use to detect any visible damage such as cracks, breaks, or defects on the edges. Its flat design allows for an application of force distributed over the contact surfaces.

What are the contraindications for the use of this instrument?

The main medical contraindication lies in the patient's known hypersensitivity or intolerance to metals, particularly to the medical stainless steel composing the instrument. Contact with the pliers could trigger an allergic reaction. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken. Furthermore, the use of the instrument is contraindicated if it shows visible signs of wear, cracks, or deformations that could compromise patient safety or the effectiveness of the surgical act.

What are the maintenance and sterilization precautions?

Helmut Zepf products are delivered non-sterile and must imperatively be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. Reprocessing must be complete to ensure asepsis. It is crucial to check for the absence of visible damage such as cracks or ruptures before any intervention. Never use damaged or worn products. Compatibility with other instruments used during surgery must also be verified beforehand by the practitioner. The number of achievable sterilization cycles depends on the care taken during cleaning and use in accordance with the manufacturer's specifications.

Who is the manufacturer and what standards are respected?

The pliers are manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer complies with strict requirements for manual stainless steel dental instruments. As a Class I device, it meets the safety and performance standards required for its intended use in dental surgery. Each instrument is identified by a unique technical reference (22.107.21) allowing for rigorous traceability within the dental office or hospital structure.


State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.

Specifications

Manufacturer Helmut Zepf
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