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Combination Instrument - Helmut Zepf (41.854.21) - Delynov

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The Instrument de Combinaison - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 41.854.21.
  • Reserved for healthcare professionals. Read instructions carefully before use.

74.67 € 74.67 EUR 74.67 € Tax Included

74.67 € Tax Included

(74.67 € / Units)
  • Manufacturer

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Instrument

What is the Helmut Zepf 41.854.21 combination instrument?

The Helmut Zepf combination instrument, referenced under code 41.854.21, is a manual dental double instrument intended for oral healthcare professionals. Manufactured from high-quality medical stainless steel, this device belongs to the category of versatile manual instruments. Its structure is specifically designed to meet the requirements of dental and implant surgery. As a product of the Helmut Zepf brand, it benefits from the expertise of Helmut Zepf Medizintechnik GmbH in the design of surgical devices. This instrument is delivered non-sterile and requires a complete preparation protocol before any clinical use.

What are the clinical indications for this instrument?

According to data from the manufacturer Helmut Zepf Medizintechnik GmbH, the intended purpose for this device is that of a manual dental instrument. It is indicated for use during various oral surgery, implantology, or periodontology procedures requiring the use of a combination instrument. Its application is strictly reserved for qualified healthcare professionals. The instrument allows for precise movements on tissues or dental structures depending on the configuration of its working ends. It is imperative to verify the suitability of the instrument with other products used during the clinical procedure to ensure optimal compatibility.

What are the technical characteristics of the device?

The Helmut Zepf combination instrument (41.854.21) is a Class I device. Its main technical characteristic lies in its manufacture from medical stainless steel, a standard material for surgical instrumentation ensuring the necessary resistance to reprocessing cycles. The product is designed to be reusable, although no maximum limit of treatment cycles is defined by the manufacturer due to the nature of the materials and design. Before each use, the practitioner must imperatively inspect the instrument to detect any visible damage, such as cracks, breaks, or defects on the cutting edges.

What are the contraindications for the use of this instrument?

The main medical contraindication mentioned by the manufacturer concerns metal intolerance. Contact with the medical stainless steel composing the instrument may cause a hypersensitivity reaction in some patients. If such a reaction occurs during the intervention, the procedure must be immediately stopped and necessary medical measures must be taken accordingly. It is therefore recommended to evaluate the patient's allergic history before any manipulation. Furthermore, the use of the instrument is prohibited if it shows signs of wear or visible damage compromising the safety of care or tissue integrity.

What are the maintenance and reprocessing precautions?

All Helmut Zepf instruments must follow a strict cleaning, disinfection, and sterilization protocol before the first use and after each subsequent use. Being delivered non-sterile, thorough cleaning is a critical step to ensure patient safety. The reprocessing process depends on the product design and the materials used. The practitioner must ensure that the instrument is perfectly clean and functional before any new intervention. It is strictly forbidden to use damaged or worn products. The durability of the device directly depends on compliance with these maintenance instructions and careful handling by healthcare personnel.

Who is the manufacturer and what standards are met?

The official manufacturer of this instrument is the company Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This medical device is classified as Class I according to current regulations. Compliance with rigorous manufacturing protocols by Helmut Zepf ensures the product's conformity with the requirements expected for manual dental instrumentation. As a Class I device, it meets the safety and performance standards defined for this category of surgical instruments. The manufacturer emphasizes the importance of verifying compatibility with other devices before any use in a clinical setting.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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