Skip to Content

Dental Descaler Instrument Tip - Helmut Zepf (24.751.123AROX) - Delynov

https://www.delynov.fr/web/image/product.template/14721/image_1920?unique=dba7abb

The Pointe pour instrument à détartrer - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.751.123AROX.
  • Reserved for healthcare professionals. Read instructions carefully before use.

61.90 € 61.9 EUR 61.90 € Tax Included

61.90 € Tax Included

(61.90 € / Units)
  • Manufacturer

This combination does not exist.

Instrument

What is the Helmut Zepf 24.751.123AROX scaling instrument tip?

The Helmut Zepf scaling instrument tip, referenced under code 24.751.123AROX, is a technical component designed for prophylaxis care. Manufactured by Helmut Zepf Medizintechnik GmbH, this instrument is crafted from high-quality medical stainless steel. It is a Class I device intended for use by healthcare professionals in a clinical setting. As a dental scaling insert, its structure is specifically studied to meet the requirements of periodontology and oral hygiene, guaranteeing efficient transmission of forces during the removal of calcified deposits.

What are the clinical indications for this insert?

This dental ultrasound insert is indicated for manual scaling and root planing procedures. Its primary use concerns the removal of calculus and calcified dental plaque, both at the supra-gingival level and in more complex sub-gingival access areas. It is used during periodontal maintenance sessions or in the initial treatment phase to sanitize the periodontium. The manufacturer Helmut Zepf specifies that this device is a manual dental instrument intended exclusively for qualified practitioners, allowing for rigorous management of prophylactic hygiene in patients who do not present contraindications to metallic components.

What are the technical characteristics of the 24.751.123AROX tip?

The Helmut Zepf scaler tip is distinguished by its manufacture in medical stainless steel, a material chosen for its resistance and compatibility with reprocessing cycles. This device is delivered non-sterile and must undergo a complete cycle of cleaning, disinfection, and sterilization before its first use, as well as between each patient. Its technical design does not define a maximum limit of treatment cycles, although the user must check for the absence of visible damage such as cracks, breaks, or wear of the cutting edges before each intervention to ensure the safety of the care.

What are the contraindications for the use of this instrument?

The main contraindication mentioned by Helmut Zepf Medizintechnik GmbH concerns hypersensitivity or intolerance to metals. Since the instrument is composed of medical stainless steel, contact with the patient may trigger an allergic reaction in sensitive individuals. In the event of a hypersensitivity reaction during the clinical procedure, the procedure must be immediately interrupted and necessary medical measures must be taken. It is therefore recommended to evaluate the patient's allergic history before using this insert to prevent any undesirable side effects related to metallic components.

What are the maintenance and reprocessing precautions?

Like any reusable Class I instrument, this tip requires a strict reprocessing protocol. Before the first use and after each procedure, the product must be cleaned, disinfected, and sterilized. Helmut Zepf emphasizes the crucial importance of visual inspection: any instrument showing signs of wear, blunt cutting edges, or micro-cracks must be discarded to avoid any risk of breakage or clinical inefficiency. Compatibility with other devices must also be verified beforehand. Due to its robust stainless steel design, there is no predefined number of cycles, as the service life depends on maintenance and usage.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer located in Seitingen-Oberflacht, Germany. This product belongs to Class I according to current medical device regulations. It meets the safety and performance requirements for manual dental instruments. The manufacturer insists that these products are reserved exclusively for trained healthcare professionals. Compliance with cleaning and sterilization protocols in accordance with the manufacturer's instructions is essential to maintain device conformity and ensure patient safety throughout its clinical life.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
Tags
Tags
Instrument