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Combination Instrument - Helmut Zepf (46.035.10)

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

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 46.035.10.
  • Reserved for healthcare professionals. Read instructions carefully before use.

73.01 € 73.01 EUR 73.01 € Tax Included

73.01 € Tax Included

(73.01 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf combined instrument (46.035.10)?

The Helmut Zepf combined instrument, referenced under code 46.035.10, is a manual dental instrument designed for healthcare professionals. Manufactured from high-quality medical stainless steel, this device belongs to the category of diagnostic and treatment instruments. Its structure typically combines two functional ends to optimize workflow during interventions. As a combined dental probe, it offers a versatile solution for tissue examination. This product is delivered non-sterile by the manufacturer Helmut Zepf Medizintechnik GmbH and requires a full preparation cycle before any clinical use.

What are the clinical indications?

This instrument is indicated for use as a manual dental instrument during various procedures in the office or operating room. It is particularly used as a dental surgery probe for the evaluation of periodontal tissues and the detection of structural anomalies. Its use is exclusively reserved for qualified healthcare professionals. It finds its application in routine examinations, periodontology, and preparatory phases of oral surgery. The design of this double periodontology instrument allows for a quick transition from an exploration function to a measurement or diagnostic function without changing tools, thus facilitating standardized clinical protocols.

What are the technical characteristics?

The Helmut Zepf instrument (46.035.10) is manufactured from medical stainless steel, ensuring resistance suitable for repeated reprocessing cycles. It is a Class I device according to current regulations. The manufacturer states that due to the product design and the materials used, there is no defined maximum limit for the number of treatment cycles achievable, although the user must inspect the instrument before each use. Characteristics include corrosion resistance subject to proper maintenance. It is imperative to check for the absence of visible damage, such as cracks, breaks, or defects on the cutting edges, before any intervention.

What are the contraindications for use?

The main medical contraindication mentioned by the manufacturer Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity to metals. An intolerance reaction may occur in some patients upon contact with the medical stainless steel of the instrument. If a hypersensitivity reaction is triggered during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken. Furthermore, the use of the instrument is strictly contraindicated if it shows visible signs of wear, cracks, or structural defects that could compromise patient safety or the effectiveness of the surgical procedure.

What are the maintenance and reprocessing precautions?

As it is a non-absorbable and reusable instrument, a strict reprocessing protocol is mandatory. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use, as well as after each subsequent use. Cleaning must be complete to remove all biological residues before the sterilization phase. It is crucial to check compatibility with other cleaning or disinfection products used. Visual examination is a key step: any instrument showing damage, excessive wear, or defective cutting edges must never be used and must be removed from service to ensure clinical safety.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This device is classified as a Class I instrument. Compliance with rigorous manufacturing protocols ensures conformity with the requirements for manual medical devices. The products are delivered non-sterile, leaving the responsibility for final sterilization to the user healthcare professional. The manufacturer emphasizes the importance of following the provided instructions for use and safety to maintain the integrity of the medical stainless steel and ensure the longevity of the instrument within the surgical arsenal.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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