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Gum scissors Helmut Zepf (46.081.16TISC) - Delynov

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The Ciseaux à gencives Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 46.081.16TISC.
  • Reserved for healthcare professionals. Read instructions carefully before use.

161.04 € 161.04 EUR 161.04 € Tax Included

161.04 € Tax Included

(161.04 € / Units)
  • Manufacturer

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Instrument

What are the Helmut Zepf 46.081.16TISC gum scissors?

Helmut Zepf gum scissors, bearing the reference 46.081.16TISC, are manual dental instruments designed for soft tissue surgery. Manufactured by Helmut Zepf Medizintechnik GmbH, these devices are crafted from high-quality medical stainless steel. They serve as essential precision tools for the practitioner during gingival cutting phases. As a Class I instrument, this equipment meets safety requirements for use in dental offices or operating rooms. Their structure is specifically designed to offer controlled handling during delicate periodontology and implantology procedures.

What are the clinical indications for these scissors?

The main indication for this manual dental instrument is the manipulation and sectioning of gingival tissues during various surgical interventions. The gum scissors are used for soft tissue excision, performing gingivectomies, or debriding flaps before suturing. In implant surgery, they allow for precise adjustment of the gum edges around healing abutments. The manufacturer Helmut Zepf specifies that the use of these instruments is strictly reserved for qualified healthcare professionals, thus ensuring application in accordance with current clinical protocols.

What are the technical characteristics of this instrument?

These gum scissors are distinguished by their medical stainless steel construction, a material chosen for its resistance and ability to withstand decontamination cycles. The technical reference 46.081.16TISC corresponds to a specific model in the Helmut Zepf Medizintechnik GmbH range. Although the product design and materials used do not allow for a defined maximum limit of processing cycles, the instrument must undergo rigorous inspection before each use. The practitioner must check for the absence of visible damage, such as cracks, breaks, or defects on the cutting edges, to ensure optimal cutting performance.

What are the contraindications for the use of these scissors?

The main contraindication mentioned by the manufacturer concerns hypersensitivity to metal components. A metal intolerance reaction in the patient may occur upon contact with the medical stainless steel of the instrument. If such a hypersensitivity reaction is triggered, the procedure must be stopped immediately and necessary medical measures must be taken. It is therefore crucial to assess the patient's allergic history before any intervention. Furthermore, the use of instruments showing signs of wear, corrosion, or structural defects is formally prohibited to avoid any risk of intraoperative complication.

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. The reprocessing process must be complete to ensure asepsis. It is very important to clean each product before use and to check compatibility with other products used. The manufacturer emphasizes that damaged or worn products must never be used. Due to the robustness of the stainless steel used, the number of achievable processing cycles depends on maintenance and handling, without a fixed limit being established by Helmut Zepf Medizintechnik GmbH.

Who is the manufacturer and what standards are respected?

These scissors are manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. The manufacturer ensures the compliance of its instruments with the safety and performance requirements for manual medical devices. Each instrument is identified by a precise reference, here code 46.081.16TISC, guaranteeing product traceability. Compliance with cleaning and sterilization protocols by the healthcare professional is essential to maintain the compliance and safety of the instrument throughout its operational life.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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