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Curette - Helmut Zepf (47.520.22) - Delynov

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

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 47.520.22.
  • Reserved for healthcare professionals. Read instructions carefully before use.

106.08 € 106.08 EUR 106.08 € Tax Included

106.08 € Tax Included

(106.08 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf (47.520.22) curette?

The Helmut Zepf curette, referenced under code 47.520.22, is a manual dental instrument designed by Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, it is intended for professional use in oral surgery. This device belongs to Class I of medical devices. Its structure is designed to offer optimal resistance during clinical interventions while guaranteeing standard biocompatibility for patients who do not present hypersensitivity to metals.

What are the clinical indications?

This manual instrument is indicated for various care and surgical procedures. Its intended purpose is to act as a manual dental instrument during phases of site cleaning, curettage of inflammatory tissues, or debridement of alveolar areas. It is used by healthcare professionals to manipulate hard or soft tissues according to the specific needs of the pathology being treated, particularly in periodontology or after an extraction to prepare the site for future implantation.

What are the technical characteristics?

The Helmut Zepf (47.520.22) curette is characterized by its medical-grade stainless steel composition, ensuring its durability after several sterilization cycles. As a Class I device, it meets safety requirements for non-invasive or short-term invasive instruments. The manufacturer specifies that due to the robust design and materials used, there is no defined maximum limit for reprocessing cycles, as long as the instrument shows no visible damage.

What are the contraindications for use?

The main contraindication lies in the patient's known hypersensitivity or intolerance to metals, specifically to the medical stainless steel used in the manufacture of the instrument. If a hypersensitivity reaction occurs during the intervention, the procedure must be stopped immediately and necessary medical measures must be taken. Furthermore, use is strictly reserved for qualified healthcare professionals mastering the associated surgical techniques.

What are the maintenance and safety precautions?

Before the first use and after each subsequent use, the Helmut Zepf curette must imperatively be cleaned, disinfected, and sterilized. The products are delivered non-sterile by Helmut Zepf Medizintechnik GmbH. It is crucial to inspect the instrument before each use to detect visible damage such as cracks, breaks, or defects on the cutting edges. The use of a damaged or worn instrument is prohibited to ensure patient safety and the effectiveness of the surgical procedure.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This recognized manufacturer respects manufacturing standards for manual dental instruments. The product is classified as a Class I medical device. Compliance with the cleaning and sterilization protocols recommended by the manufacturer is essential to maintain the conformity of the device during its repeated use in dental offices or hospital environments.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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