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Instrument axial for fillings - Helmut Zepf (26.200.36) - Delynov

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The Instrument axial pour plombages - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 26.200.36.
  • Reserved for healthcare professionals. Read instructions carefully before use.

44.51 € 44.51 EUR 44.51 € Tax Included

44.51 € Tax Included

(44.51 € / Units)
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Instrument

What is the Helmut Zepf axial filling instrument?

The Helmut Zepf axial instrument, referenced under code 26.200.36, is a manual instrument specifically designed for restorative dentistry procedures. Manufactured by Helmut Zepf Medizintechnik GmbH, this device is made of high-quality medical stainless steel to guarantee its resistance during clinical interventions. As a filling instrument, its axial structure is optimized to facilitate access to various dental cavities. This device is classified as a Class I instrument according to current regulations, highlighting its professional use in dental practices for the implementation of filling materials.

What are the clinical indications for this instrument?

The intended use of this manual dental instrument primarily concerns the stages of coronal restoration. It is indicated for the transport, application, and modeling of filling materials within prepared cavities. Its axial design allows the practitioner to exert the controlled pressure necessary for material condensation, thus ensuring optimal marginal adaptation. Whether for direct restorations or intermediate phases of conservative care, this Helmut Zepf instrument meets the technical requirements of dental surgeons during daily care protocols.

What are the technical characteristics of instrument 26.200.36?

The Helmut Zepf axial instrument is distinguished by its manufacture in medical stainless steel, a material chosen for its biocompatibility and durability. Its technical reference 26.200.36 corresponds to a specific axial configuration allowing for ergonomics adapted to precision work. This product is delivered non-sterile by the manufacturer Helmut Zepf Medizintechnik GmbH. Before any use, it is imperative to carry out a complete cycle of cleaning, disinfection, and sterilization. Its robust design allows it to withstand repeated reprocessing cycles, although a visual inspection to detect any cracks or defects on the edges is mandatory before each clinical procedure.

What are the contraindications for the use of this filling instrument?

The main contraindication mentioned by the manufacturer concerns known hypersensitivity or metal intolerance. Since the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. If a hypersensitivity reaction occurs during the procedure, the practitioner must immediately stop the intervention and take the necessary medical measures. In addition, it is strictly contraindicated to use an instrument showing visible damage such as breaks, cracks, or pronounced wear on the active parts, in order to guarantee patient safety and the effectiveness of the treatment.

What are the maintenance and sterilization precautions?

Like any Class I instrument intended for dental surgery, this Helmut Zepf device requires a rigorous reprocessing protocol. Products must be cleaned, disinfected, and sterilized before the first use as well as after each subsequent use. Due to its design and the materials used, there is no defined maximum limit for treatment cycles, but the longevity of the instrument depends on compliance with the manufacturer's safety instructions. The user must check compatibility with other cleaning products and ensure the absence of defects on the instrument surfaces before integrating it into their technical tray.

Who is the manufacturer and what standards are respected?

This instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. The device complies with the regulations for Class I medical devices. The manufacturer specifies that the instrument is intended exclusively for qualified healthcare professionals. Traceability and manufacturing quality are ensured by compliance with European standards applicable to manual stainless steel dental instruments. Each product is identified by a unique reference (26.200.36) allowing for precise tracking within the dental practice or hospital structure.


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Specifications

Manufacturer Helmut Zepf
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