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Interchangeable Periotome Tip - Helmut Zepf (26.182.31) - Delynov

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The Pointe de périotome interchangeable - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 26.182.31.
  • Reserved for healthcare professionals. Read instructions carefully before use.

78.09 € 78.09 EUR 78.09 € Tax Included

78.09 € Tax Included

(78.09 € / Units)
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Instrument

What is the Helmut Zepf interchangeable periotome tip?

The Helmut Zepf interchangeable periotome tip, referenced under code 26.182.31, is a manual instrument designed by Helmut Zepf Medizintechnik GmbH. Manufactured from medical stainless steel, this periotome tip is intended to be mounted on a specific handle for oral surgical procedures. Its structure allows for precise insertion into the periodontal space. Unlike monobloc instruments, this interchangeable system offers flexibility in maintenance and replacement of the working part. It belongs to the category of surgical consumables and meets the manufacturing requirements of a recognized manufacturer in the high-tech dental instrumentation sector.

What are the clinical indications for this instrument?

This periotome tip is primarily indicated for sectioning periodontal ligaments (desmodontium) prior to dental extraction. In oral and implant surgery, its use allows for the detachment of fibrous attachments without damaging the surrounding alveolar bone, which is crucial for preserving the bone plate for immediate or delayed implant placement. It is used by healthcare professionals during simple or complex extraction procedures, allowing for easier luxation of the tooth or root. The instrument is specifically designed to penetrate the narrow space between the root and the alveolar bone.

What are the technical characteristics of the 26.182.31 tip?

The Helmut Zepf interchangeable periotome tip (reference 26.182.31) is designed in high-quality medical stainless steel. It is characterized by a thin, tapered working part optimized for passage through the periodontal ligament. This device is delivered non-sterile by Helmut Zepf Medizintechnik GmbH, which requires a complete processing protocol before the first use. As a Class I instrument, it must undergo systematic verification of the surface condition and cutting edges before each procedure. Its design allows for repeated cleaning, disinfection, and sterilization, although no maximum cycle limit is defined by the manufacturer; visible wear should dictate its replacement.

What are the contraindications for the use of this device?

The main medical contraindication mentioned by the manufacturer Helmut Zepf concerns hypersensitivity or intolerance to metals. Being manufactured from medical stainless steel, contact with the instrument may trigger a reaction in patients allergic to certain components of the alloy. If such a hypersensitivity reaction occurs during the surgical act, the procedure must be stopped immediately and necessary clinical measures must be taken. Apart from this specific contraindication, use is reserved exclusively for qualified healthcare professionals mastering dental and periodontal surgery techniques.

What are the maintenance and reprocessing precautions?

All Helmut Zepf instruments must be cleaned, disinfected, and sterilized before the first use and after each subsequent use. It is imperative to check for the absence of visible damage such as cracks, breaks, or defects on the cutting edges. The use of a damaged or worn periotome tip is prohibited as it could compromise patient safety or the effectiveness of the surgical gesture. The reprocessing process must follow standard hospital or dental office sterilization protocols. Due to its design and the materials used, the lifespan of the tip depends on clinical use and compliance with maintenance instructions.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, located in Seitingen-Oberflacht, Germany. This product is classified as a Class I medical device according to current regulations. As a manual instrument, it complies with the rigorous manufacturing standards imposed on medical devices (MDR). The manufacturer specifies that compatibility with other products (such as periotome handles) must be verified by the practitioner before use. Helmut Zepf ensures the traceability and quality of its instruments, guaranteeing that the stainless steel used meets safety requirements for temporary contact with human tissues during dental care.


State of the art

Surgical medical consumables play a decisive role in operative safety.

Specifications

Manufacturer Helmut Zepf
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