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Small Acrylic Glass Bar - Helmut Zepf (24.926.75) - Delynov

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The Barre petite en verre acrylique - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 24.926.75.
  • Reserved for healthcare professionals. Read instructions carefully before use.

35.21 € 35.21 EUR 35.21 € Tax Included

35.21 € Tax Included

(35.21 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf small acrylic glass bar?

The small acrylic glass bar, referenced under code 24.926.75 by Helmut Zepf, is an acrylic glass storage accessory designed for the dental environment. This device is presented as a compact and transparent support, allowing for the structuring of the workspace during surgical or prosthetic acts. Manufactured by Helmut Zepf Medizintechnik GmbH, it meets the organizational needs of practitioners looking for a dental mixing accessory or a storage support for small elements. Its acrylic structure ensures excellent visibility of the contents while offering resistance suitable for daily use in the practice.

What are the clinical indications for this accessory?

As a manual dental instrument, this accessory is indicated for the storage and preparation of materials within the operating block or treatment room. It can be used as an acrylic glass mixing bar for the preparation of various components required for implantology or periodontology procedures. Its compact format is ideal for the temporary storage of small devices or for organizing supplies during an intervention. Although its specific use is not detailed beyond its manual function, its design makes it a versatile tool for maintaining asepsis and order on the technical tray.

What are the technical characteristics of this product?

The Helmut Zepf small bar (ref. 24.926.75) is characterized by the use of acrylic glass as the main material, offering transparency and lightness. This product belongs to the CONSO category and is classified as a Class I medical device according to current regulations. Delivered non-sterile by the manufacturer Helmut Zepf Medizintechnik GmbH, this accessory requires a full cycle of cleaning, disinfection, and sterilization before its first use and after each subsequent use. Its simple design allows for effective reprocessing, although no maximum limit of cycles is defined by the manufacturer; visible wear should be the criterion for replacement.

What are the contraindications for the use of this device?

According to the manufacturer Helmut Zepf data, the main contraindication concerns metal intolerance in the patient. Although the main accessory is made of acrylic glass, contact with the medical stainless steel parts of the associated instrumentation can trigger a hypersensitivity reaction. If such a reaction occurs during the procedure, use must be immediately discontinued and necessary medical measures must be taken. It is also strictly advised against using the product if it shows visible damage such as cracks, breaks, or structural defects that could compromise the safety of care or hygiene.

What are the maintenance and reprocessing precautions?

Reprocessing the acrylic glass bar is a critical step since the products are delivered non-sterile. Before the first use, and between each patient, the accessory must be fully cleaned, disinfected, and sterilized. The practitioner must verify compatibility with other cleaning products used. Due to the nature of the materials, it is imperative to inspect the accessory for any signs of wear or degradation before each use. The use of damaged products is prohibited. The sterilization process must follow standard protocols for reusable medical devices to ensure total microbiological safety.

Who is the manufacturer and what standards are respected?

The device is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This product complies with Class I medical device regulations. The manufacturer emphasizes that the use of this instrument is strictly reserved for qualified healthcare professionals. Compliance with safety instructions, particularly systematic cleaning and sterilization before use, is mandatory to ensure compliance with public health requirements. Traceability is ensured by the technical reference 24.926.75, allowing precise identification of the lot and manufacturer specifications within the Helmut Zepf range.


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Manufacturer Helmut Zepf
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