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Radicular Canal Spreader - Helmut Zepf (19.513.05) - Delynov

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The Écarteur de canal radiculaire - Helmut Zepf is a medical device manufactured by Helmut Zepf Medizintechnik GmbH.

  • Compliance: Medical device Class I.
  • Manufacturer: Helmut Zepf Medizintechnik GmbH.
  • Reference: 19.513.05.
  • Reserved for healthcare professionals. Read instructions carefully before use.

41.37 € 41.37 EUR 41.37 € Tax Included

41.37 € Tax Included

(41.37 € / Units)
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Instrument

What is the Helmut Zepf root canal retractor?

The Helmut Zepf root canal retractor, bearing the reference 19.513.05, is a specialized manual instrument used in endodontic microsurgery. Manufactured by Helmut Zepf Medizintechnik GmbH, this device is designed in high-quality medical stainless steel to guarantee the structural strength necessary during tissue retraction. As an instrument in the INSTRU category, it features an architecture adapted to the constraints of the oral space, allowing the practitioner to effectively clear the surgical field. This device is delivered non-sterile and requires a complete cleaning, disinfection, and sterilization protocol before its first use and between each patient.

What are the clinical indications for this retractor?

This root canal retractor is primarily indicated for endodontic surgery procedures, such as apicoectomies or the treatment of periapical lesions. Its role is to keep mucoperiosteal flaps away from the drilling or resection area, thus ensuring soft tissue protection and increased visibility of the root apex. In oral surgery, its use is crucial to secure access to deep anatomical structures while minimizing visual interference. It is intended exclusively for professional use by dental surgeons or endodontic specialists trained in invasive surgical techniques.

What are the technical characteristics of reference 19.513.05?

The Helmut Zepf 19.513.05 instrument is characterized by its manufacture in medical stainless steel, a material chosen for its biocompatibility and its ability to undergo repeated sterilization cycles. Although the specific design of the working end is optimized for endodontic retraction, the manufacturer specifies that due to the nature of the materials and the intended use, there is no defined maximum limit of processing cycles, as long as the instrument does not show visible damage. It is imperative to check for the absence of cracks, breaks, or defects on the edges before each procedure to ensure patient safety and the effectiveness of the surgical movement.

What are the contraindications for the use of this instrument?

The main medical contraindication documented by Helmut Zepf Medizintechnik GmbH concerns known hypersensitivity or metal intolerance in the patient. Contact of medical stainless steel with tissues can trigger an allergic reaction in sensitive subjects. If such a hypersensitivity reaction occurs during the intervention, the procedure must be immediately interrupted and necessary medical measures must be taken. It is the practitioner's responsibility to validate the patient's history regarding possible allergies to metallic components before any use of this root canal retractor in the mouth.

What are the maintenance and reprocessing precautions?

Like any reusable Class I instrument, the endodontic retractor must follow a strict reprocessing protocol. As Helmut Zepf products are delivered non-sterile, they must be cleaned, disinfected, and sterilized before the first use. The manufacturer emphasizes the importance of cleaning each product before proceeding to final sterilization. A thorough visual inspection is required to detect any premature wear or structural damage. The use of a damaged instrument is prohibited. Compatibility with other cleaning products or sterilization devices must also be verified in advance by qualified medical personnel.

Who is the manufacturer and what standards are respected?

The retractor is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized company located in Seitingen-Oberflacht, Germany. This medical device belongs to Class I according to current regulations. The manufacturer complies with safety and performance requirements for manual instruments intended for dental surgery. Traceability is ensured by technical reference 19.513.05. As a Class I device, it meets the rigorous manufacturing standards imposed for non-invasive or short-term invasive surgical instruments, thus guaranteeing constant reliability during demanding clinical endodontic procedures.


State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.

Specifications

Manufacturer Helmut Zepf
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