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Curved Metzenbaum Scissors 14.5cm - Helmut Zepf (46.431.14TISC) - Delynov

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The Ciseaux courbes de Metzenbaum de 14.5cm - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 46.431.14TISC.
  • Reserved for healthcare professionals. Read instructions carefully before use.

145.90 € 145.9 EUR 145.90 € Tax Included 286.01 €

145.90 € Tax Included 286.01 €

(0.00 € / Units)
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Instrument

What are the Helmut Zepf 14.5cm curved Metzenbaum scissors?

The 14.5cm curved Metzenbaum scissors, referenced under code 46.431.14TISC by Helmut Zepf, are Class I surgical instruments intended for clinical practice. Manufactured in medical stainless steel by Helmut Zepf Medizintechnik GmbH, these instruments are distinguished by their curved structure adapted for fine dissection. This device belongs to the category of manual instruments that are non-sterile upon delivery. Its stainless steel design guarantees resistance suitable for the reprocessing cycles required in dental and oral surgery practices, while providing the precision required for handling soft tissues and suture auxiliaries.

What are the clinical indications for these scissors?

According to the manufacturer's specifications from Helmut Zepf, these scissors are indicated as a medical instrument intended to separate and cut biological tissues. In oral and implant surgery, they are used for precise dissection of flaps and sectioning of soft tissues. Beyond tissue aspects, these scissors are also intended for cutting surgical aids, notably suture threads and drainage tubes. Their specific curvature allows easier access to certain areas of the oral cavity, thus facilitating the practitioner's work during resection or suture finishing phases.

What are the technical characteristics of this device?

These Metzenbaum scissors (reference 46.431.14TISC) feature a length of 14.5cm, a standard dimension for oral surgery interventions. They are manufactured from high-quality medical stainless steel by Helmut Zepf Medizintechnik GmbH. The product is classified as a Class I medical device. It is delivered non-sterile and requires a complete protocol of cleaning, disinfection, and sterilization before the first use as well as between each patient. The manufacturer specifies that due to the design and materials used, there is no defined maximum limit for processing cycles, as long as the instrument does not show visible damage.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by Helmut Zepf concerns metal intolerance. Contact with this medical stainless steel instrument can cause a hypersensitivity reaction in certain sensitive patients. If such an allergic or intolerance reaction manifests during the intervention, the manufacturer stipulates that the procedure must be immediately stopped and necessary medical measures must be taken. It is therefore essential to check the patient's allergic history before any use. Furthermore, the use of the instrument is strictly reserved for qualified healthcare professionals mastering the associated surgical techniques.

What are the maintenance and safety precautions?

Patient safety and instrument longevity depend on rigorous maintenance. All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the very first use and after each subsequent use. It is imperative to visually inspect the scissors before each intervention to detect possible damage or signs of wear, such as cracks, breaks, or defects on the cutting edges. The manufacturer formally prohibits the use of damaged or worn products. Additionally, compatibility with other products used during the procedure must be verified beforehand to ensure optimal surgical safety.

Who is the manufacturer and what standards are respected?

This medical device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. As a Class I instrument, it meets the regulatory requirements in force for medical devices (MDR). The manufacturer ensures traceability and production quality through strict protocols. The products are delivered non-sterile, leaving the responsibility for final reprocessing to the healthcare professional. Compliance with the cleaning and sterilization instructions issued by Helmut Zepf is essential to maintain device conformity throughout its life cycle in a clinical environment.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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